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
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
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
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.
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
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to food additives, herbicides and insecticides including muscle weakness, skin irritation, poor muscle coordination, headache, cough, diarrhea, dizziness, fatigue, fever, stomach pain and vomiting.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS & USAGE SECTION Eye Floaters Formulated for associated symptoms such as dark or grey specks and strings or cobwebs of material floating within the field of vision.
INDICATIONS: For temporary relief of symptoms related to chemical toxicity including fatigue, frequent colds, insomnia, headache, rash, depression, sinusitis, constipation, poor circulation, and memory difficulties.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS & USAGE SECTION Tinnitus Formulated for associated symptoms such as ringing, buzzing, echoing, pressure, pain, throbbing and sensitivity to noise.
INDICATIONS & USAGE SECTION Tobacco Withdrawal Formulated for symptoms associated with tobacco use such as anxiety, cravings, irritability, respiratory conditions and stress caused by abstinence.
INDICATIONS: For temporary relief of allergic rhinitis with runny nose, nasal mucus with yellow green discharge, pain and swelling of sinus cavities and postnasal drip.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to Herxheimer reactions such as brain fog, fatigue, chills, muscle discomfort, nausea, and malaise.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Ear Care Echinacea, Hydrastis canadensis, Apis mellifica, Arsenicum album, Belladonna, Bryonia, Capsicum annuum, Causticum, Cinchona officinalis, Conium maculatum, Dulcamara, Ferrum phosphoricum, Hepar sulphuris calcareum, Kali sulphuricum, Lycopodium clavatum, Mercurius vivus, Mezereum, Phosphorus, Plantago major, Pulsatilla, Silicea, Verbascum thapsus, Tellurium metallicum, Influenzinum INFLUENZA B VIRUS INFLUENZA B VIRUS ECHINACEA, UNSPECIFIED ECHINACEA, UNSPECIFIED FERROSOFERRIC PHOSPHATE FERROSOFERRIC PHOSPHATE APIS MELLIFERA APIS MELLIFERA ARSENIC TRIOXIDE ARSENIC CATION (3+) ATROPA BELLADONNA ATROPA BELLADONNA BRYONIA ALBA ROOT BRYONIA ALBA ROOT CAPSICUM CAPSICUM CAUSTICUM CAUSTICUM CINCHONA OFFICINALIS BARK CINCHONA OFFICINALIS BARK CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP SOLANUM DULCAMARA TOP SOLANUM DULCAMARA TOP POTASSIUM SULFATE POTASSIUM CATION LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE MERCURY MERCURY DAPHNE MEZEREUM BARK DAPHNE MEZEREUM BARK PHOSPHORUS PHOSPHORUS SUCROSE SILICON DIOXIDE SILICON DIOXIDE PLANTAGO MAJOR PLANTAGO MAJOR ANEMONE PULSATILLA ANEMONE PULSATILLA TELLURIUM TELLURIUM VERBASCUM THAPSUS VERBASCUM THAPSUS INFLUENZA A VIRUS INFLUENZA A VIRUS CALCIUM SULFIDE CALCIUM SULFIDE GOLDENSEAL GOLDENSEAL
INDICATIONS & USAGE SECTION Formulated for associated symptoms such as gas, bloating, fatigue, mental fogginess, itching, discharge and other related symptoms.
INDICATIONS: For temporary relief of minor aches and pains in muscles and joints, fever with dryness of mucous membranes and dry cough; muscular soreness and fatigue with headache.
Stage Fright-Fear Passiflora incarnata, Valeriana officinalis, Aconitum napellus, Anacardium orientale, Argentum nitricum, Arsenicum album, Cypripedium pubescens, Gelsemium sempervirens, Ignatia amara, Kali carbonicum, Lycopodium clavatum, Natrum muriaticum, Phosphorus, Sambucus nigra, Sepia, Staphysagria, Stramonium, Tarentula hispana, Theridion WATER ALCOHOL PASSIFLORA INCARNATA FLOWERING TOP PASSIFLORA INCARNATA FLOWERING TOP SEMECARPUS ANACARDIUM JUICE SEMECARPUS ANACARDIUM JUICE SILVER NITRATE SILVER CATION ARSENIC TRIOXIDE ARSENIC CATION (3+) CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT CYPRIPEDIUM PARVIFLORUM VAR. PUBESCENS ROOT GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT STRYCHNOS IGNATII SEED STRYCHNOS IGNATII SEED POTASSIUM CARBONATE CARBONATE ION LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE SODIUM CHLORIDE SODIUM CATION PHOSPHORUS PHOSPHORUS SAMBUCUS NIGRA FLOWERING TOP SAMBUCUS NIGRA FLOWERING TOP SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE DELPHINIUM STAPHISAGRIA SEED DELPHINIUM STAPHISAGRIA SEED DATURA STRAMONIUM DATURA STRAMONIUM LYCOSA TARANTULA LYCOSA TARANTULA THERIDION CURASSAVICUM THERIDION CURASSAVICUM VALERIAN VALERIAN ACONITUM NAPELLUS ACONITUM NAPELLUS
INDICATIONS & USAGE SECTION Formulated for symptoms associated with performance anxiety such as apprehension, nausea, restlessness, trembling and over-sensitivity.
Wellness Defense Echinacea (Angustifolia), Allium Cepa, Bryonia (Alba), Gelsemium Sempervirens, Sanguinaria Canadensis, Eupatorium Perfoliatum, Kali Bichromicum, Phosphorus, Aconitum Napellus, Influenzinum 2017-2018 ECHINACEA ANGUSTIFOLIA WHOLE ECHINACEA ANGUSTIFOLIA ONION ONION BRYONIA ALBA ROOT BRYONIA ALBA ROOT GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT EUPATORIUM PERFOLIATUM FLOWERING TOP EUPATORIUM PERFOLIATUM FLOWERING TOP POTASSIUM DICHROMATE DICHROMATE ION PHOSPHORUS PHOSPHORUS ACONITUM NAPELLUS WHOLE ACONITUM NAPELLUS INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180A (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED) INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180A (H1N1) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) INFLUENZA A VIRUS A/HONG KONG/4801/2014 X-263B (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED) INFLUENZA A VIRUS A/HONG KONG/4801/2014 X-263B (H3N2) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) INFLUENZA B VIRUS B/BRISBANE/60/2008 ANTIGEN (PROPIOLACTONE INACTIVATED) INFLUENZA B VIRUS B/BRISBANE/60/2008 HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) ECHINACEA ANGUSTIFOLIA ROOT ANHYDROUS LACTOSE MAGNESIUM STEARATE H
INDICATIONS: For the temporary relief of runny nose, congestion, sore throat, headache, nausea, cough, body aches, fever and chills. Best taken at first sign of immune imbalance.
INDICATIONS: For temporary relief of diarrhea (painless, clay colored); eczema with itching; hay fever, offensive discharge running from the nose, and dyspepsia with bitter taste.