INDICATIONS: May temporarily relieve sinus congestion due to hay fever and allergic rhinitis.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
USES: May temporarily relieve: •sinus congestion •runny nose •sneezing** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
By Generic Name
Drugs with the same generic name (different brands)
USES: May temporarily relieve: •sinus congestion •runny nose •sneezing** **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 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
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 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
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.
Uses: For the temporary relief of minor aches and pains of muscles and joints, associated with simple backache, arthritis, strains, bruises, and sprains.
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
INDICATIONS: For temporary relief of flushes of heat with attacks of perspiration, physical weakness with headaches, moodiness with symptoms ever-changing.
Adrenal Support Aralia Quinquefolia, Humulus Lupulus, Adrenalinum, Cortisone Aceticum, Thyroidinum (Suis), Selenium Metallicum, Arsenicum Album, Calcarea Carbonica, Convallaria Majalis, Crotalus Horridus, Ferrum Metallicum, Nux Vomica, Phosphorus, Sepia, Phosphoricum Acidum AMERICAN GINSENG AMERICAN GINSENG HOPS HOPS EPINEPHRINE EPINEPHRINE CORTISONE ACETATE CORTISONE THYROID, PORCINE SUS SCROFA THYROID SELENIUM SELENIUM ARSENIC TRIOXIDE ARSENIC CATION (3+) OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE CONVALLARIA MAJALIS CONVALLARIA MAJALIS CROTALUS HORRIDUS HORRIDUS VENOM CROTALUS HORRIDUS HORRIDUS VENOM IRON IRON STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHOSPHORUS PHOSPHORUS SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE PHOSPHORIC ACID PHOSPHORIC ACID WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to hypoadrenalism including fatigue, nervous exhaustion, anxiety, and forgetfulness.** **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 sinusitis infection including sinus/nasal congestion, cough, earache, mucous congestion in the middle ear, sneezing and vaccination reaction.
Cardioforce II Abrotanum, Boldo, Cimicifuga Racemosa, Convallaria Majalis, Kali Phosphoricum, Taraxacum Officinale, Magnesia Sulphurica, Oleander, Natrum Muriaticum, Bellis Perennis ARTEMISIA ABROTANUM FLOWERING TOP ARTEMISIA ABROTANUM FLOWERING TOP PEUMUS BOLDUS LEAF PEUMUS BOLDUS LEAF BLACK COHOSH BLACK COHOSH CONVALLARIA MAJALIS CONVALLARIA MAJALIS POTASSIUM PHOSPHATE, DIBASIC PHOSPHATE ION TARAXACUM OFFICINALE TARAXACUM OFFICINALE MAGNESIUM SULFATE HEPTAHYDRATE MAGNESIUM CATION NERIUM OLEANDER LEAF NERIUM OLEANDER LEAF SODIUM CHLORIDE CHLORIDE ION BELLIS PERENNIS BELLIS PERENNIS WATER ALCOHOL
INDICATIONS: For temporary relief of symptoms related to parasite infestation including diarrhea, colic, vermifuge, digestive aid, flatulence, intestinal problems, constipation, spasms, gallstones, colitis, and jaundice.
Lymph-Tone II Homeopathic Liquid HORSE CHESTNUT HORSE CHESTNUT AZADIRACHTA INDICA BARK AZADIRACHTA INDICA BARK BARIUM CARBONATE BARIUM CATION BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK PEUMUS BOLDUS LEAF PEUMUS BOLDUS LEAF BUFO BUFO CUTANEOUS GLAND BUFO BUFO CUTANEOUS GLAND OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION COENZYME A COENZYME A COLLINSONIA CANADENSIS ROOT COLLINSONIA CANADENSIS ROOT ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA FERRUM PHOSPHORICUM FERROSOFERRIC PHOSPHATE SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND BOS TAURUS HYPOTHALAMUS BOS TAURUS HYPOTHALAMUS WOOD CREOSOTE WOOD CREOSOTE NADIDE NADIDE SODIUM CHLORIDE CHLORIDE ION PHOSPHORUS PHOSPHORUS PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT PINUS SYLVESTRIS LEAFY TWIG PINUS SYLVESTRIS LEAFY TWIG SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND PINE TAR PINE TAR PULSATILLA VULGARIS PULSATILLA VULGARIS SILICON DIOXIDE COLLOIDAL SILICON DIOXIDE STILLINGIA SYLVATICA ROOT STILLINGIA SYLVATICA ROOT THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG WATER ALCOHOL GLYCERIN
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.
Sinus Complex Antimonium tartaricum, Echinacea angustifolia, Euphorbium officinarum, Hepar sulphuris calcareum, Hepatica tribola, Hydrastis canadensis, Mercurius sulfuratus ruber, Natrum muriaticum, Phosphorus ANTIMONY POTASSIUM TARTRATE ANTIMONY ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA EUPHORBIA RESINIFERA RESIN EUPHORBIA RESINIFERA RESIN CALCIUM SULFIDE CALCIUM CATION HEPATICA NOBILIS VAR. OBTUSA HEPATICA NOBILIS VAR. OBTUSA GOLDENSEAL GOLDENSEAL MERCURIC SULFIDE MERCURIC CATION SODIUM CHLORIDE SODIUM CATION PHOSPHORUS PHOSPHORUS ALCOHOL
Indications: A homeopathic remedy for the temporary relief of symptoms due to overgrowth of Candida albicans yeast, such as: yeast infections thrush nail fungus constipation headache nausea itchy skin fatigue diarrhea flatulence forgetfulness sleeplessness cravings Indications: Un remede homeopathique pour le soulagement temporaire des symptomes dus a la proliferation de la levure Candida albicans, tels que: infections a la levure muguet mycose des ongles constipation maux de tete nausees demangeaisons fatigue dearrhee flatulences perte de memoire insomnie et fringales
HOMEOPATHIC INDICATIONS: For the temporary relief of the symptoms of nausea and vomiting associated with pain, pregnancy, vertigo, headache, gastroenteritis and odors.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS AND USAGE For temporary relief of nausea with headache, dry cough, and constriction of the chest.
Sambucol Cold and Flu Nasal Relief Bryonia, Gelsemium Sempervirens, Sabucus Nigra, Sulphur, Zincum Gluconicum BRYONIA ALBA ROOT BRYONIA ALBA ROOT GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT SAMBUCUS NIGRA FLOWERING TOP SAMBUCUS NIGRA FLOWERING TOP SULFUR SULFUR ZINC GLUCONATE ZINC CATION BLACK CARROT ANTHOCYANINS CROSCARMELLOSE SODIUM LACTOSE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE SUCROSE EUROPEAN ELDERBERRY JUICE off purple off grey color with specks SCF Elderberry