USES: • For the temporary relief of symptoms including: • symptoms of heavy metal toxicity • stomach inflammation • cough • poor concentration • nausea • vomiting • occasional diarrhea • stomach pain • headache • sweating • metallic taste These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HUIZHOU JINSHENG MEDICAL TECHNOLOGY CO., LTD
FDA
OTC
Straighten the cleaning solution Pour it into the cleaning position for cleaning Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes,ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.
Saline Solution is intended for use in OTC ear,nose,and throat devices intended specifically to administer medicinal substances to treat ear,nose,and throat disorders.These instruments include the powder blower,dropper,ear wick,manual nebulizer pump,and nasal inhaler. If using with an OTC ear,nose,or throat device,the follow the directions provided with the device and only use as directed.
HUIZHOU JINSHENG MEDICAL TECHNOLOGY CO., LTD
FDA
OTC
Usage: This product is designed for gentle cleaning of the face, mouth, nose, eyes, ears, and wounds. It can also be used with a nebulizer to help relieve discomfort in the nose and mouth.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
0.9% Sodium Chloride Injection, USP solution is sterile and nonpyrogenic. It is a parenteral solution containing sodium chloride in water for injection intended for intravenous administration. For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1,000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solution is a parenteral fluid and electrolyte replenisher. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for injection, USP is chemically designated H2O. The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (freeflex® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP solutions are sterile and nonpyrogenic. They are parenteral solutions containing various concentrations of sodium chloride in water for injection intended for intravenous administration. For 0.45% Sodium Chloride Injection, USP, each 100 mL contains 450 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 77 mEq; chloride 77 mEq. The osmolarity is 154 mOsmol/L (calc.). For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection. Electrolytes per 1000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.). The pH for both concentrations in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers. The solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded. The solutions are parenteral fluid and electrolyte replenishers. Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water. Water for Injection, USP is chemically designated H2O. The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C (77°F) during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. It contains no antimicrobial agents. The pH ranges from 4.5 to 7.0. Composition, osmolarity, and ionic concentration are shown below: 0.9% Sodium Chloride Injection, USP contains 9 g/L Sodium Chloride, USP (NaCl) with an osmolarity of 308 mOsmol/L (calc). It contains 154 mEq/L sodium and 154 mEq/L chloride. The FLEBOFLEX and FLEBOFLEX LUER plastic containers are fabricated from latex-free polyolefins or polypropylene plastic materials. The solution contact materials do not contain PVC, DEHP, or other plasticizers. The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. The suitability of the container materials has been established through biological evaluations, which have shown the containers pass Class VI U.S. Pharmacopeia (USP) testing for plastic containers. These tests confirm the biological safety of the container systems.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
This preparation is designed solely for parenteral use only after addition of drugs that require dilution or must be dissolved in an aqueous vehicle prior to injection. 0.9% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, isotonic solution of sodium chloride and water for injection. Each mL contains sodium chloride 9 mg. It contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers to dilute or dissolve drugs for injection. 0.308 mOsmol/mL (calc.). 0.9% Sodium Chloride Injection, USP contains no preservatives. The solution may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. pH 5.3 (4.5 to 7.0). Sodium Chloride, USP is chemically designated NaCl, a white crystalline compound freely soluble in water. The glass container is a Type I borosilicate glass and meets the requirements of the powdered glass test according to the USP standards. The semi-rigid vial is fabricated from a specially formulated polyolefin. It is a copolymer of ethylene and propylene. The safety of the plastic has been confirmed by tests in animals according to USP biological standards for plastic containers. The container requires no vapor barrier to maintain the proper drug concentration.
INDICATIONS: For weight management and inflammation support. This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
3% Sodium Chloride Injection, USP is a sterile, nonpyrogenic, hypertonic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. The pH may have been adjusted with hydrochloric acid. It contains no antimicrobial agents. Composition, ionic concentration, osmolarity, and pH are shown in Table 1 . Table 1. *Normal physiological osmolarity range is approximately 280 to 310 mOsmol/L. Size (mL) Composition (g/L) Ionic Concentration (mEq/L) *Osmolarity (mOsmol/L) (calc) pH Sodium Chloride, USP (NaCl) Sodium Chloride 3% Sodium Chloride Injection, USP 500 30 513 513 1,027 5.0 (4.5 to 7.0) The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (free flex ® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.
4 Kids Cold and Cough DaytimeONION CALCIUM SULFIDE SODIUM CHLORIDE PHOSPHORUS PULSATILLA VULGARIS SULFUR AND GOLDENSEAL
Uses* ■ Helps temporarily relieve symptoms of common cold in children at night, including: ■ cough ■ runny nose ■ post nasal drip ■ sneezing ■ sore throat ■ nasal or chest congestion ■ occasional sleeplessness
Uses ■ Helps temporarily relieve symptoms of common cold in children at night, including: ■ cough ■ runny nose ■ post nasal drip ■ sneezing ■ sore throat ■ nasal or chest congestion ■ occasional sleeplessness
4 Kids Cold and Mucus NighttimeEUPHRASIA STRICTASILICON DIOXIDE RUMEX CRISPUS ROOT ANEMONE PULSATILLA GOLDENSEAL SODIUM CHLORIDE PHOSPHORUS ONION BRYONIA ALBA ROOT MATRICARIA CHAMOMILLA ARABICA COFFEE BEAN CALCIUM SULFIDE AND SULFUR
Uses Temporarily relieves the symptoms of the common cold in children especially at night including accumulation of mucus in chest, throat and nose, cough with mucus, runny nose, sneezing, nasal congestion and occasional sleeplessness.
4 KIDS COLD N COUGH GRAPE FLAVORONION CALCIUM SULFIDE GOLDENSEAL SODIUM CHLORIDE PHOSPHORUS ANEMONE PULSATILLA AND SULFUR
Uses ■Temporarily relieves symptoms of common cold in children, including: ■ accumulation of mucus in chest, throat or nose ■ cough with expectoration of thick, discolored mucus ■ runny nose ■ sneezing ■ nasal or chest congestion
INDICATIONS: For temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. Remedy #1 supports detoxification and cellular repair.
Uses For temporary relief of symptoms: minor anxiety fear irritability nervousness minor mood swings restlessness stage fright nervous stomach oversensitivity As per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image: 911.jpg
INDICATIONS FOR USE: for the temporary relief of nerve pain symptoms including: • itching • numbness • swelling • burning • cramping • tingling Product indications are based solely on Homeopathic Materia Medica and have not been evaluated by the FDA.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to consumption of grains, soy, and gluten, including bowel irregularity, occasional diarrhea, occasional constipation, and fatigue.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Human Papilloma Virus Homochord Human Papilloma Nosode HUMAN PAPILLOMAVIRUS HUMAN PAPILLOMAVIRUS WATER ALCOHOL
INDICATIONS: For the temporary relief of symptoms related to Human Papilloma Virus including itching in the pelvic area.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of bloating of the stomach, flatulence or rhinitis.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
HOMEOPATHIC INDICATIONS: Temporary relief of symptoms related to hormone imbalances or insufficiencies in men and women, including low energy, inability to handle stress, trouble focusing, changes in mood, infertility, irregular menstrual cycles (females) and lack of libido.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
D3 Organ Support Conium Maculatum, Dulcamara, Echinacea (Angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbicum Acidum, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (Vulgaris), Sarcolacticum Acidum, Lymph Node (Suis), Sulphur, Glandula Suprarenalis Suis, Phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (Suis), Spleen (Suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Glyphosate, Funiculus Umbilicalis Suis, Tonsil (Suis) CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP SOLANUM DULCAMARA TOP SOLANUM DULCAMARA TOP ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA HORSE CHESTNUT HORSE CHESTNUT ANTIMONY POTASSIUM TARTRATE ANTIMONY CATION (3+) ASCORBIC ACID ASCORBIC ACID PROTORTONIA CACTI PROTORTONIA CACTI GALIUM APARINE GALIUM APARINE GENTIANA LUTEA ROOT GENTIANA LUTEA ROOT GERANIUM ROBERTIANUM GERANIUM ROBERTIANUM ANEMONE PULSATILLA ANEMONE PULSATILLA LACTIC ACID, L- LACTIC ACID, L- SUS SCROFA LYMPH SUS SCROFA LYMPH SULFUR SULFUR SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PHENYLALANINE PHENYLALANINE TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION FERROSOFERRIC PHOSPHATE FERROSOFERRIC PHOSPHATE PORK LIVER PORK LIVER SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS SUS SCROFA SPLEEN SUS SCROFA SPLEEN CORTISONE ACETATE CORTISONE MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS BARIUM CARBONATE BARIUM CATION GLYPHOSATE GLYPHOSATE SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA TONSIL SUS SCROFA TONSIL SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS LIOTHYRONINE LIOTHYRONINE SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW BISPHENOL A BISPHENOL A BROMINE BROMINE CHLORINE CHLORINE HYDROFLUORIC ACID FLUORIDE ION IODINE IODINE ESCHERICHIA COLI ESCHERICHIA COLI WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to improper breakdown and excretion of allergenic substances, including pain, fatigue, cramping and upper respiratory allergy.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Sambucol Cold and Flu Relief Bryonia, Gelsemium sempervirens, Sabucus nigra, Sulphur, Zincum gluconicum BRYONIA ALBA ROOT BRYONIA ALBA ROOT SAMBUCUS NIGRA FLOWERING TOP SAMBUCUS NIGRA FLOWERING TOP GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT BLACK CARROT ANTHOCYANINS MAGNESIUM STEARATE ZINC GLUCONATE ZINC CATION CROSCARMELLOSE SODIUM EUROPEAN ELDERBERRY JUICE MALTODEXTRIN SULFUR SULFUR LACTOSE, UNSPECIFIED FORM MICROCRYSTALLINE CELLULOSE SUCROSE SCF off purple off grey color with specks Elderberry
Uses Temporarily relieves cold & flu symptoms. Provides temporary relief from respiratory symptoms such as sneezing, runny nose, nasal & sinus congestion, minor sore throat and headache. Also temporarily relieves body aches associated with the flu.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to toxicity caused by environmental substances including neck pain, hives, occasional constipation, cough, and headache.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: May temporarily relieve sore throat, extreme fatigue, glandular swelling and mucous discharge.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Ileocecal Valve Support Iodium, Hypophysis Suis, Thyroidinum, (Suis), Glandula Suprarenalis Suis, Fel Tauri, Taraxacum Officinale, Bryonia (Alba), Carbo Vegetabilis, Colocynthis, Indolum, Lycopodium Clavatum, Mercurius Corrosivus, Nux Vomica, Phosphorus, Pulsatilla (Vulgaris) IODINE IODINE SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND SUS SCROFA THYROID SUS SCROFA THYROID SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND BOS TAURUS BILE BOS TAURUS BILE TARAXACUM OFFICINALE TARAXACUM OFFICINALE BRYONIA ALBA ROOT BRYONIA ALBA ROOT ACTIVATED CHARCOAL ACTIVATED CHARCOAL CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP INDOLE INDOLE LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE MERCURIC CHLORIDE MERCURIC CATION STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHOSPHORUS PHOSPHORUS PULSATILLA VULGARIS ANEMONE PULSATILLA WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Ileocecal Valve dysfunction including pelvic pain, fever, headache, bad breath, ringing in the ears, occasional diarrhea, and occasional constipation.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Leg Cramp Relief Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album CAUSTICUM CAUSTICUM CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP COPPER COPPER MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF TIN TIN VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT LACTOSE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE convex ML
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to vaccinations including fever, headache, muscle pain, rash, cough, lethargy, and aching back.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For temporary relief of low back pain, dry mouth, infrequent urination, headache, low energy levels.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to the cleansing and detoxifying of the liver, such as poor digestion, irregularity and low energy levels.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of swelling due to minor injury.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to common bacterial infections (respiratory and urinary tract infections, food poisoning) such as fever, headache, mucous congestion, stomach discomfort, cough, joint discomfort, and occasional diarrhea.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.