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 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.
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 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.
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.
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
911 Adrenal Burnout and FatigueACETICUM AC ADRENALINUM ADRENOCORTICOTROPHIN 30X AESCULUS HIPPOCASTANUM FLOS ALFALFA ALPHA LIPOIC AC AMBRA ARG NIT AVENA SATIVA BRYONIA CARBONEUM OXYGENISATUM CARPINUS BETULUS FLOS DNA FUMARICUM ACIDUM GELSEMIUM SEMPERVIRENS HEPAR SULPHURIS CALCAREUM HYPOTHALAMUS KALI PHOSPHORICUM LACTICUM ACIDUM LECITHIN NATRUM MURIATICUM OXALICUM ACIDUM PHOSPHORICUM ACIDUM PITUITARUM POSTERIUM SARCOLACTICUM ACIDUM SELENIUM METALLICUM SEPIA SILICEA SUCCINICUM ACIDUM AND THYROIDINUM.
Uses † for temporary relief of: physical fatigue mental and emotional fatigue nervous exhaustion sluggish mind poor concentration weariness confusion apathy irritability indifference body aches lack of focus eyes sensitive to light digestive symptoms caused by stress light-headed upon standing up † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.
INDICATIONS: May temporarily relieve symptoms associated with lymphatic congestion, such as tendency to catch colds, fluid retention, and fatigue.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Reflux RxS Acetyl Coenzyme A, ATP, Nadidum, Coumarinum, Argentum Nitricum, Ipecacuanha, Robinia Pseudoacacia, Sulphur COENZYME A COENZYME A ADENOSINE TRIPHOSPHATE ADENOSINE TRIPHOSPHATE NADIDE NADIDE COUMARIN COUMARIN SILVER NITRATE SILVER CATION IPECAC IPECAC ROBINIA PSEUDOACACIA BARK ROBINIA PSEUDOACACIA BARK SULFUR SULFUR STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED OREGANO LEAF OIL OREGANO LEAF OIL SUS SCROFA DUODENUM SUS SCROFA DUODENUM SUS SCROFA ESOPHAGUS SUS SCROFA ESOPHAGUS SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA STOMACH SUS SCROFA STOMACH CENTAURIUM ERYTHRAEA CENTAURIUM ERYTHRAEA PEPSIN PEPSIN HYDROCHLORIC ACID HYDROCHLORIC ACID ANHYDROUS CITRIC ACID ANHYDROUS CITRIC ACID FORMIC ACID FORMIC ACID LACTIC ACID, L- LACTIC ACID, L- PROTEUS MORGANII PROTEUS MORGANII WATER ALCOHOL
HOMEOPATHIC INDICATIONS: Temporary relief of symptoms such as upper abdomen pain, flatulence, exercise induced tenderness.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
USES: Temporarily relieves blistering rash.** ** These statements have not been reviewed by the FDA. They are based on traditional homeopathic practice. Temporarily relieves blistering rash.**
Amethyst 8104 Amethyst CALCIUM FLUORIDE FLUORIDE ION ALCOHOL WATER
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to heartburn and esophageal reflux.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Grain and Soy Allergen Mix Adenosinum Triphosphoricum Dinatrum, Quercetin, Rutin, Ileum (Suis), Jejunum (Suis) Stomach (Suis), Bacillus Thuringiensis (BT Toxin), Gluten, Amaranth, Avena Sativa, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Cortisone Aceticum, Glyphosate, Sycotic Co Bacillus ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE QUERCETIN QUERCETIN RUTIN RUTIN SODIUM CARBONATE CARBONATE ION SUS SCROFA ILEUM SUS SCROFA ILEUM SUS SCROFA JEJUNUM SUS SCROFA JEJUNUM SUS SCROFA STOMACH SUS SCROFA STOMACH WHEAT GLUTEN WHEAT GLUTEN AMARANTH AMARANTH ACID AVENA SATIVA FLOWERING TOP AVENA SATIVA FLOWERING TOP SODIUM SULFATE SODIUM SULFATE ANHYDROUS LACTIC ACID, L- LACTIC ACID, L- ELYMUS REPENS ROOT ELYMUS REPENS ROOT CORTICOTROPIN CORTICOTROPIN GLYPHOSATE GLYPHOSATE ENTEROCOCCUS FAECALIS ENTEROCOCCUS FAECALIS WATER ALCOHOL
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.
Appetite Control Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (Suis), Bacopa Speciosa, Equol, Gambogia, Oxytocin Acetate, Rhodiola, Stomach (Suis), Chininum Sulphuricum, Iodium, Lycopodium Clavatum, Phosphorus, Dopamine Hydrochloride, Thyroidinum (Suis), Cina, Serotonin (Hydrochloride), Morgan Gaertner ACETYL COENZYME A ACETYL COENZYME A ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE SUS SCROFA ADRENAL CORTEX SUS SCROFA ADRENAL CORTEX BACOPA MONNIERI WHOLE BACOPA MONNIERI WHOLE EQUOL, (+/-)- EQUOL, (+/-)- OXYTOCIN ACETATE OXYTOCIN SEDUM ROSEUM ROOT SEDUM ROSEUM ROOT SUS SCROFA STOMACH SUS SCROFA STOMACH QUININE SULFATE QUININE IODINE IODINE LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE PHOSPHORUS PHOSPHORUS DOPAMINE HYDROCHLORIDE DOPAMINE SUS SCROFA THYROID SUS SCROFA THYROID ARTEMISIA CINA PRE-FLOWERING TOP ARTEMISIA CINA FLOWER SEROTONIN HYDROCHLORIDE SEROTONIN SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms including constant appetite, increased or insatiable hunger.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Slim Lycopodium clavatum, Phytolacca decandra, Abies canadensis, Ammonium bromatum, Ammonium muriaticum, Pulsatilla, Kali bichromicum, Ammonium carbonicum, Fucus vesiculosus, LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT AMMONIUM BROMIDE BROMIDE ION TSUGA CANADENSIS BARK TSUGA CANADENSIS BARK AMMONIUM CHLORIDE AMMONIUM CATION PULSATILLA VULGARIS WHOLE ANEMONE PULSATILLA POTASSIUM DICHROMATE DICHROMATE ION AMMONIUM CARBONATE AMMONIUM CATION FUCUS VESICULOSUS FUCUS VESICULOSUS CAPSICUM CAPSICUM SILVER NITRATE SILVER CATION SILICON DIOXIDE SILICON DIOXIDE BOS TAURUS ADRENAL GLAND BOS TAURUS ADRENAL GLAND CALCIUM ARSENATE ARSENATE ION IRON IRON ANTIMONY TRISULFIDE ANTIMONY TRISULFIDE OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE GRAPHITE GRAPHITE POTASSIUM CARBONATE CARBONATE ION SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE IODINE IODINE THYROID SUS SCROFA THYROID WATER ALCOHOL
HOMEOPATHIC INDICATIONS: Temporary relief of symptoms related to Iron in foods and supplements, including fatigue, cramping and jitteriness.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Chalcedony 8108 Chalcedony CHALCONE CHALCONE ALCOHOL WATER
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to heartburn and esophageal reflux.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: Temporary relief of symptoms related to improper levels of stomach acid, including heartburn, dyspepsia and bowel irregularity.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Krebs Stimulator Plus Tabebuia impetiginosa, Uncaria tomentosa, Hypothalamus (Suis), Pituitaria glandula (Suis), Glandula suprarenalis suis, Nadidum, Lacticum acidum, Sarcolacticum acidum, TABEBUIA IMPETIGINOSA BARK TABEBUIA IMPETIGINOSA BARK CAT'S CLAW CAT'S CLAW SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND NADIDE NADIDE LACTIC ACID, L- LACTIC ACID, L- COENZYME A COENZYME A UBIDECARENONE UBIDECARENONE GERMANIUM SESQUIOXIDE GERMANIUM SESQUIOXIDE ADENOSINE TRIPHOSPHATE DISODIUM ADENOSINE TRIPHOSPHATE WATER ALCOHOL
INDICATIONS: Enhances electron transport systems and absorption of oxygen into the cell. Indicated in any condition involving the damaging effect of oxidation, which also increases free radical damage. Should be used with detoxosodes for maximum benefit. Symptoms of a Krebs cycle deficiency may include fatigue, muscle weakness and pain.