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
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
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.
12 CELL SALTS COMPLEXCALCAREA FLUORICA CALCAREA PHOSPHORICA CALCAREA SULPHURICA FERRUM PHOSPHORICUM KALI MURIATICUM KALI PHOSPHORICUM KALI SULPHURICUM MAGNESIA PHOSPHORICA NATRUM MURIATICUM NATRUM PHOSPHORICUM NATRUM SULPHURICUM SILICEA
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.
365 Everyday Value Be Well Cough EaseANTIMONY POTASSIUM TARTRATE BRYONIA ALBA ROOT PROTORTONIA CACTI DROSERA ROTUNDIFOLIA IPECAC PULSATILLA VULGARIS RUMEX CRISPUS ROOT PONGIA OFFICINALIS SKELETON ROASTED LOBARIA PULMONARIA
USES* temporary relieves cough due to minor throat and bronchial irritation as may occur with a cold helps relieve chest congestion due to common colds by loosening phlegm (mucus) and thinning bronchial secretions to make coughs more productive
365 Everyday Value Be Well Cough Ease for KidsANTIMONY POTASSIUM TARTRATE BRYONIA ALBA ROOT PROTORTONIA CACTI DROSERA ROTUNDIFOLIA IPECAC PULSATILLA VULGARIS RUMEX CRISPUS ROOT PONGIA OFFICINALIS SKELETON ROASTED LOBARIA PULMONARIA
Temporary relieves cough due to minor throat and bronchial irritation as may occur with a cold. Helps loosen phlegms (mucus) and thin bronchial secretions to make coughs more productive.
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 for fast relief of symptoms: fever, sweats, chills, aches, nausea, restlessness. If fever lasts for more than three days, or if symptoms change, consult a doctor. Contains no aspirin, acetaminophen, or ibuprofen.
INDICATIONS AND USAGE For temporary relief of symptoms related to Pertussis infection including cough, bronchial congestion and difficult breathing, fever, whooping cough and vaccination reactions.
Uses *For temporary relief of symptoms of common eye irritations: mineral accumulations, tearing, light sensitivity, eye fatigue, redness, and itching. *This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.
Rejuvenate 2000 Maximum Strength Formula For Men rSomatotropin, rIGF-I, rIGF-II, RNA, DNA,Glandula Suprarenalis Suis, Hepar Suis, Pituitarium Posterium, Thymus, Thyroidinum, Placenta Totalis Suis, Orchitinum, Abrotanum, Anacard Or, Arsenicum Alb, Baryta Carb, Baryta Mur, Calc Carb, Calc Phos, Ferrum Met, Fucus, Hekla, Hellebor Nig, Ignatia, Lycopodium, Nicotinamidium, Secale, Silicea, Cobaltum Met, Lithium Carb, Mag Phos, Mang Acet, Kali Phos, Selenium Met, Zinc Met. SOMATROPIN SOMATROPIN DALOTUZUMAB DALOTUZUMAB SACCHAROMYCES CEREVISIAE RNA SACCHAROMYCES CEREVISIAE RNA HERRING SPERM DNA HERRING SPERM DNA SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND SUS SCROFA THYMUS SUS SCROFA THYMUS THYROID, UNSPECIFIED THYROID, UNSPECIFIED SUS SCROFA PLACENTA SUS SCROFA PLACENTA SUS SCROFA TESTICLE SUS SCROFA TESTICLE ARTEMISIA ABROTANUM FLOWERING TOP ARTEMISIA ABROTANUM FLOWERING TOP SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE ARSENIC TRIOXIDE ARSENIC CATION (3+) BARIUM CARBONATE BARIUM CATION BARIUM CHLORIDE DIHYDRATE BARIUM CATION OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE TRIBASIC CALCIUM PHOSPHATE PHOSPHATE ION IRON IRON FUCUS VESICULOSUS FUCUS VESICULOSUS HEKLA LAVA HEKLA LAVA HELLEBORUS NIGER ROOT HELLEBORUS NIGER ROOT STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE NIACINAMIDE NIACINAMIDE CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM SILICON DIOXIDE SILICON DIOXIDE COBALT COBALT LITHIUM CARBONATE LITHIUM CATION MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION MANGANESE ACETATE TETRAHYDRATE MANGANESE POTASSIUM PHOSPHATE, DIBASIC PHOSPHATE ION SELENIUM SELENIUM ZINC ZINC WATER ALCOHOL GLYCERIN
Uses for temporary relief of symptoms associated with herbicide and pesticide exposure: headaches, physical and mental weakness, nausea, diarrhea, dizziness, respiratory difficulties.
Indications and Usage Uses for symptomatic relief of: indigestion, bloating, gas, abdominal discomforts after eating. Assists natural gall bladder function. Promotes flow of bile.
Uses for temporary relief of pain in the foot, heel, toes and joints including: swelling, burning, itching, tingling, tearing pains, throbbing, cramps, shooting pains.
TOTAL FLU CLD 1 Arsenicum alb, Baptisia, Bryonia, Causticum, Cinchona, Dulcamara, Echinacea purp, Eucalyptus, Eupatorium perf, Gelsemium, Influenzinum, Lachesis, Phytolacca, Rhus tox, Sarcolacticum ac, Sulphur, Wyethia, Anas barbariae ARSENIC TRIOXIDE ARSENIC CATION (3+) BAPTISIA TINCTORIA ROOT BAPTISIA TINCTORIA ROOT BRYONIA ALBA ROOT BRYONIA ALBA ROOT CAUSTICUM CAUSTICUM CINCHONA BARK CINCHONA BARK SOLANUM DULCAMARA TOP SOLANUM DULCAMARA TOP ECHINACEA PURPUREA ECHINACEA PURPUREA EUCALYPTUS GLOBULUS LEAF EUCALYPTUS GLOBULUS LEAF EUPATORIUM PERFOLIATUM FLOWERING TOP EUPATORIUM PERFOLIATUM FLOWERING TOP GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT INFLUENZA A VIRUS INFLUENZA A VIRUS LACHESIS MUTA VENOM LACHESIS MUTA VENOM PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF LACTIC ACID, L- LACTIC ACID, L- SULFUR SULFUR WYETHIA HELENIOIDES ROOT WYETHIA HELENIOIDES ROOT CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE ALCOHOL WATER
Uses For temporary relief of symptoms: Low back, leg, hip, and joint pain Nerve inflammation Numbness and tingling Weakness in back and legs 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: Sciatic Nerve Formula.jpg
Female Discomforts Apis mellifica, Belladonna, Borax, Bryonia, Calcarea phosphorica, Cantharis, Hydrastis canadensis, Kali bichromicum, Lac caninum, Pulsatilla, Sepia, Thuja occidentalis APIS MELLIFERA APIS MELLIFERA ATROPA BELLADONNA ATROPA BELLADONNA SODIUM BORATE BORATE ION BRYONIA ALBA ROOT BRYONIA ALBA ROOT TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION LYTTA VESICATORIA LYTTA VESICATORIA GOLDENSEAL GOLDENSEAL POTASSIUM DICHROMATE DICHROMATE ION CANIS LUPUS FAMILIARIS MILK CANIS LUPUS FAMILIARIS MILK PULSATILLA PRATENSIS PULSATILLA PRATENSIS SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG WATER ANHYDROUS CITRIC ACID POTASSIUM SORBATE
Uses for temporary relief of vaginal discomforts associated with yeast overgrowth or irritations: itching, burning, discharges, soreness, dryness, and swelling.
Uses for temporary relief of symptoms associated with arthritic pain: rheumatic pain, stiff and swollen joints, body aches, weakness, and pain in any joint.
Indications: For temporary relief of: •body aches & pains •nasal congestion •headaches & fevers associated with the common cold and flu. Use according to label indications under standard homeopathic indications.
Neobryxol Ultra Asterias rubens, Bryonia alba, Conium maculatum Galium aparine, Hoang-nan, Lachesis, Ledum palustre, Nux Vomica, Ova tosta and Viscum album. ASTERIAS RUBENS ASTERIAS RUBENS BRYONIA ALBA ROOT BRYONIA ALBA ROOT CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP GALIUM APARINE GALIUM APARINE STRYCHNOS WALLICHIANA BARK STRYCHNOS WALLICHIANA BARK LACHESIS MUTA VENOM LACHESIS MUTA VENOM LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED EGG SHELL, COOKED EGG SHELL, COOKED VISCUM ALBUM WHOLE VISCUM ALBUM WHOLE WATER ALCOHOL
Indications and Usage Maintains the system under the stress of malignancy regardless of location. Modulate cancerous action, tumors, targets tissues that tend to be more susceptible to cancer, neuralgias, and dropsy of extremities, and rheumatic pains. Based on the homeopathic Materia Medicas. Reference image ultra.jpg
Uses* Uses*: For temporary relief of symptoms of common eye irritations: mineral accumulations, tearing, light sensitivity, eye fatigue, redness, itching. *This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.