INDICATIONS: For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
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
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
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
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.
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.
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
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to gingivitis, inflamed and bleeding gums and minor pain.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: May temporarily relieve symptoms associated with decreased lymphatic drainage of the organs, such as fatigue, headache, lymphatic swelling, and bad effects from sedentary habits.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Sugar and Food Additive Allergen Mix Cinnamic Acid, Aspartame, Ileum (Suis), Jejunum (Suis), Stomach (Suis), Phloridzinum, Adenosinum Triphosphoricum Dinatrum, Argentum Nitricum, Fructose, Glucose, Lycopodium Clavatum, Saccharum Lactis, Saccharum Officinale, Sarcolacticum Acidum, High Fructose Corn Syrup, Malvin, Adrenocorticotrophin, Dysentery Bacillus, Maple Sugar, Morgan Gaertner CINNAMIC ACID CINNAMIC ACID ASPARTAME ASPARTAME SUS SCROFA ILEUM SUS SCROFA ILEUM SUS SCROFA JEJUNUM SUS SCROFA JEJUNUM SUS SCROFA STOMACH SUS SCROFA STOMACH PHLORIZIN PHLORIZIN ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE SILVER NITRATE SILVER CATION FRUCTOSE FRUCTOSE ANHYDROUS DEXTROSE ANHYDROUS DEXTROSE LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE LACTOSE ANHYDROUS LACTOSE SUCROSE SUCROSE LACTIC ACID, L- LACTIC ACID, L- HIGH FRUCTOSE CORN SYRUP HIGH FRUCTOSE CORN SYRUP MALVIN MALVIN CORTICOTROPIN CORTICOTROPIN SHIGELLA DYSENTERIAE SHIGELLA DYSENTERIAE ACER SACCHARUM SAP ACER SACCHARUM SAP PROTEUS MORGANII PROTEUS MORGANII WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to allergies to sugars and food additives in foods and supplements including fatigue, headaches and nervousness.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. Remedy #1 supports detoxification and cellular repair.
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.
INDICATIONS: For temporary relief of symptoms related to increased appetite, regulation of fat metabolism, headache, fatigue, and detoxification stress.
Gynetox Angelica Archangelica, Cimicifuga Racemosa, Zincum Gluconicum, Funiculus Umbilicalis Suis, Lymph Node (Suis), Oophorinum (Suis), Uterus (Suis), Glandula Suprarenalis Suis, Thyroidinum Suis, Boricum Acidum, Kreosotum, Mercurius Solubilis, Pulsatilla, Sepia, Calcarea Carbonica, Phosphorus, Sabina, Candida Albicans, Herpes Simplex 1 And 2 Nosode, Human Papilloma Virus Nosode ANGELICA ARCHANGELICA ROOT ANGELICA ARCHANGELICA ROOT BLACK COHOSH BLACK COHOSH ZINC GLUCONATE ZINC CATION SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA LYMPH SUS SCROFA LYMPH SUS SCROFA OVARY SUS SCROFA OVARY SUS SCROFA UTERUS SUS SCROFA UTERUS SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND SUS SCROFA THYROID SUS SCROFA THYROID BORIC ACID BORIC ACID WOOD CREOSOTE WOOD CREOSOTE MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS ANEMONE PULSATILLA ANEMONE PULSATILLA SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE PHOSPHORUS PHOSPHORUS JUNIPERUS SABINA LEAFY TWIG JUNIPERUS SABINA LEAFY TWIG CANDIDA ALBICANS CANDIDA ALBICANS HUMAN HERPESVIRUS 1 HUMAN HERPESVIRUS 1 HUMAN HERPESVIRUS 2 HUMAN HERPESVIRUS 2 HUMAN PAPILLOMAVIRUS HUMAN PAPILLOMAVIRUS WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to Bartonella such as achiness, malaise, headache, chills, backache, abdominal pain, brain fog, and neck and face discomfort.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
BioTox Hep Cochlearia Armoracia, Chelidonium Majus, Arsenicum Album, Hepar Suis, Spleen (Suis), Thymus (Suis), Hepatitis C Nosode, Hepatitis A Nosode, Hepatitis B Nosode HORSERADISH HORSERADISH CHELIDONIUM MAJUS WHOLE CHELIDONIUM MAJUS ARSENIC TRIOXIDE ARSENIC CATION (3+) PORK LIVER PORK LIVER SUS SCROFA SPLEEN SUS SCROFA SPLEEN SUS SCROFA THYMUS SUS SCROFA THYMUS HEPATITIS C VIRUS HEPATITIS C VIRUS HEPATITIS A VIRUS HEPATITIS A VIRUS HEPATITIS B VIRUS HEPATITIS B VIRUS WATER ALCOHOL
INDICATIONS For the temporary relief of bloating, gas, anxiousness, insomnia, or occasional headache due to sensitivity to phenolic compounds found in foods or other products.*
INDICATIONS: For support of symptoms of food and environmental sensitivities or intolerances due to slight errors in diet and exposure. May include mood changes, headaches, bloating, gas, and irritation in digestion.
HGH Young Again Agnus Castus, Ambra Grisea, Petroselinum Sativum, Estradiol, L-Dopa, Melatonin, Testosterone, Adenosinum Triphosphoricum Dinatrum, alpha-Lipoicum Acidum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Ubidecarenonum, Baryta Carbonica, Conium Maculatum, Selenium Metallicum, Folliculinum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus Suis, Lymph Node (Suis), Medulla Ossis Suis, Oophorinum (Suis), Orchitinum (Suis), Pancreas Suis, Spleen (Suis), Human Growth Hormone, CHASTE TREE CHASTE TREE AMBERGRIS AMBERGRIS PETROSELINUM CRISPUM PETROSELINUM CRISPUM ESTRADIOL ESTRADIOL LEVODOPA LEVODOPA MELATONIN MELATONIN TESTOSTERONE TESTOSTERONE ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE THIOCTIC ACID .ALPHA.-LIPOIC ACID NADIDE NADIDE PANTOTHENIC ACID PANTOTHENIC ACID LACTIC ACID, L- LACTIC ACID, L- UBIDECARENONE UBIDECARENONE BARIUM CARBONATE BARIUM CATION CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP SELENIUM SELENIUM ESTRONE ESTRONE SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER SUS SCROFA LYMPH SUS SCROFA LYMPH SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW SUS SCROFA OVARY SUS SCROFA OVARY SUS SCROFA TESTICLE SUS SCROFA TESTICLE SUS SCROFA PANCREAS SUS SCROFA PANCREAS SUS SCROFA SPLEEN SUS SCROFA SPLEEN SOMATROPIN SOMATROPIN APIOLE (PARSLEY) APIOLE (PARSLEY) PROTEUS MORGANII PROTEUS MORGANII WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to aging including fatigue, minor joint pain and muscle soreness.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Leaky Gut Formula Alfalfa, Fragaria Vesca, Glycyrrhiza Glabra, Aloe, Astacus Fluviatilis, Berberis Aquifolium, Lac Defloratum, Natrum Carbonicum, Saccharum Officinale, Fel Tauri, Pancreas Suis, Pepsinum, Antimonium Crudum, Carbo Vegetabilis, Euphorbium Officinarum, Lycopodium Clavatum, Magnesia Carbonica, Zincum Metallicum, Colibacillinum Cum Natrum Muriaticum, Proteus (Mirabilis) ALFALFA ALFALFA ALPINE STRAWBERRY ALPINE STRAWBERRY GLYCYRRHIZA GLABRA GLYCYRRHIZA GLABRA ALOE ALOE ASTACUS ASTACUS ASTACUS ASTACUS BERBERIS AQUIFOLIUM ROOT BARK BERBERIS AQUIFOLIUM ROOT BARK SKIM MILK SKIM MILK SODIUM CARBONATE CARBONATE ION SUCROSE SUCROSE BOS TAURUS BILE BOS TAURUS BILE SUS SCROFA PANCREAS SUS SCROFA PANCREAS PEPSIN PEPSIN ANTIMONY TRISULFIDE ANTIMONY TRISULFIDE ACTIVATED CHARCOAL ACTIVATED CHARCOAL EUPHORBIA RESINIFERA RESIN EUPHORBIA RESINIFERA RESIN LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE MAGNESIUM CARBONATE CARBONATE ION ZINC ZINC ESCHERICHIA COLI ESCHERICHIA COLI PROTEUS MIRABILIS PROTEUS MIRABILIS WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to leaky gut syndrome such as fatigue, seasonal allergies, joint pain, occasional constipation, mental fogginess and occasional diarrhea.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: May temporarily relieve symptoms associated with exhaustion, joint pain, and immune weakness.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to skin infections including inflammation, rash, fever and swelling.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.