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
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.
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.
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
INDICATIONS: For temporary relief of minor pain and stiffness due to arthritis.** **These statements are based up traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of symptoms due to joint inflammation and swelling.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: May temporarily relieve pains throughout shoulder joint, arm, fingers and small joints, swelling and tenderness of the fingers and toe joints, inflammation.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
INDICATIONS: For temporary relief of fever, irritated throat and cough due to bacterial and viral conditions. **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Leg Cramp Relief Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album CAUSTICUM CAUSTICUM CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP COPPER COPPER MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF TIN TIN VERATRUM ALBUM ROOT VERATRUM ALBUM ROOT LACTOSE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE convex ML
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to toxicity caused by environmental substances including neck pain, hives, occasional constipation, cough, and headache.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For symptom relief due to environmental toxin exposure.** **These statements are based upon traditional homeopathic practices. They have not been reviewed by the Food and Drug Administration.
Natural Fit Kali Phosphoricum, Natrum Sulphuricum, Agnus Castus, Chelidonium Majus, Fucus Vesiculosus, Lycopodium Clavatum, Thuja Occidentalis, Capsicum Annuum, Carduus Marianus, Cysteinum, Hydrocotyle Asiatica, Kali Carbonicum, Nux Vomica, Phytolacca Decandra, Rosa Canina, Flos, Salix Alba, Thea Sinensis, Gambogia, Carbo Vegetabilis, Calcarea Carbonica, Graphites, Natrum Muriaticum, Natrum Phosphoricum, Glandula Suprarenalis Suis, Hepar Suis, Pancreas Suis, Pituitarum Posterium (Bovine), Placenta Totalis Suis, DIBASIC POTASSIUM PHOSPHATE PHOSPHATE ION SODIUM SULFATE SODIUM SULFATE ANHYDROUS CHASTE TREE FRUIT CHASTE TREE FRUIT CHELIDONIUM MAJUS WHOLE CHELIDONIUM MAJUS WHOLE FUCUS VESICULOSUS FUCUS VESICULOSUS LYCOPODIUM CLAVATUM SPORE LYCOPODIUM CLAVATUM SPORE THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG CAPSICUM CAPSICUM MILK THISTLE MILK THISTLE CYSTEINE CYSTEINE CENTELLA ASIATICA WHOLE CENTELLA ASIATICA POTASSIUM CARBONATE CARBONATE ION STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT ROSA CANINA FLOWER ROSA CANINA FLOWER SALIX ALBA BARK SALIX ALBA BARK GREEN TEA LEAF GREEN TEA LEAF GAMBOGE GAMBOGE ACTIVATED CHARCOAL ACTIVATED CHARCOAL OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE GRAPHITE GRAPHITE SODIUM CHLORIDE CHLORIDE ION SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE PHOSPHATE ION SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER SUS SCROFA PANCREAS SUS SCROFA PANCREAS BOS TAURUS PITUITARY GLAND, POSTERIOR BOS TAURUS PITUITARY GLAND SUS SCROFA PLACENTA SUS SCROFA PLACENTA THYROID, BOVINE THYROID, BOVINE GYMNEMA SYLVESTRE LEAF GYMNEMA SYLVESTRE LEAF WATER WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms of stress such as terror, horror, post traumatic stress, fight or flight response, recurring nightmares, difficulty sleeping, difficulty concentrating, restlessness, and easy irritability.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: Supports healthy mineral and electrolyte balance. Improves absorption of vitamins from food. Helps replenish body with vital nutrients after strenuous workout. May decrease general pain and nervousness.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Vermasode Abrotanum, Artemisia Vulgaris, Cina, Juglans Nigra, Spigelia Anthelmia, Teucrium Marum, Sabadilla, Silicea, Tanacetum Vulgare, Graphites, Influenzinum, Morbillinum, Diphtherinum, Mononucleosis Virus Nosode, Epstein-Barr Virus Nosode, Herpes Zoster Nosode, Poliomyelitis Nosode, Haemophilus, Hepatitis A Nosode, Hepatitis C Nosode, Pneumococcinum, Coxsackie A2, A7, B1, B3, B4 Nosode ARTEMISIA ABROTANUM FLOWERING TOP ARTEMISIA ABROTANUM FLOWERING TOP ARTEMISIA VULGARIS ROOT ARTEMISIA VULGARIS ROOT ARTEMISIA CINA PRE-FLOWERING TOP ARTEMISIA CINA FLOWER BLACK WALNUT BLACK WALNUT SPIGELIA ANTHELMIA SPIGELIA ANTHELMIA TEUCRIUM MARUM TEUCRIUM MARUM SCHOENOCAULON OFFICINALE SEED SCHOENOCAULON OFFICINALE SEED SILICON DIOXIDE COLLOIDAL SILICON DIOXIDE TANACETUM VULGARE TOP TANACETUM VULGARE TOP GRAPHITE GRAPHITE INFLUENZA A VIRUS INFLUENZA A VIRUS INFLUENZA B VIRUS INFLUENZA B VIRUS MEASLES VIRUS MEASLES VIRUS DIPHTHERIAL RESPIRATORY PSEUDOMEMBRANE HUMAN DIPHTHERIAL RESPIRATORY PSEUDOMEMBRANE HUMAN HUMAN HERPESVIRUS 4 HUMAN HERPESVIRUS 4 HUMAN HERPESVIRUS 3 HUMAN HERPESVIRUS 3 POLIOVIRUS POLIOVIRUS HAEMOPHILUS INFLUENZAE TYPE B HAEMOPHILUS INFLUENZAE TYPE B HEPATITIS A VIRUS HEPATITIS A VIRUS HEPATITIS C VIRUS HEPATITIS C VIRUS STREPTOCOCCUS PNEUMONIAE STREPTOCOCCUS PNEUMONIAE HUMAN COXSACKIEVIRUS A2 HUMAN COXSACKIEVIRUS A2 HUMAN COXSACKIEVIRUS A7 HUMAN COXSACKIEVIRUS A7 HUMAN COXSACKIEVIRUS B1 HUMAN COXSACKIEVIRUS B1 HUMAN COXSACKIEVIRUS B3 HUMAN COXSACKIEVIRUS B3 HUMAN COXSACKIEVIRUS B4 HUMAN COXSACKIEVIRUS B4 WATER ALCOHOL