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
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
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.
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
7 Select Redness ReliefGLYCERIN AND NAPHAZOLINE HCI
Directions to open bottle, push cap down and twist counter-clockwise instill 1 to 2 drops in the affected eye(s) up to four time daily children under 6 years of age: ask a doctor
INDICATIONS & USAGE: For temporary relief of minor burning and soreness upon urination, mild pain in the region of the right kidney, swelling of the legs, and scanty urination.
INDICATIONS: May temporarily relieve weakness and exhaustion, minor abdominal cramps, bloating, and vomiting.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to minor injuries including bruises, contusions, lesions, sprains, dislocations, fractures, and trauma following surgery.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
ALLERSODE II Allium Cepa, Ambrosia Artemisiaefolia, Euphrasia Officinalis, Sabadilla, Alfalfa, American Elm, American Sycamore, Ash, American Beech, Black Walnut, Black Willow, Box Elder, Eastern Cottonwood, False Ragweed, Giant Ragweed, Goldenrod, Kentucky Bluegrass, Orchard Grass, Red Birch, Red Clover, Red Oak, Redtop Grass, Hickory, Sheep Sorrel, Short Ragweed, Timothy Grass, Western Ragweed, Yellow Dock, Glandula Suprarenalis Suis, Hepar Suis, Histaminum Hydrochloricum, Arsenicum Album, Phosphorus ONION ONION AMBROSIA ARTEMISIIFOLIA AMBROSIA ARTEMISIIFOLIA EUPHRASIA STRICTA EUPHRASIA STRICTA SCHOENOCAULON OFFICINALE SEED SCHOENOCAULON OFFICINALE SEED RUMEX ACETOSELLA POLLEN RUMEX ACETOSELLA POLLEN RUMEX CRISPUS TOP RUMEX CRISPUS TOP POA PRATENSIS TOP POA PRATENSIS TOP DACTYLIS GLOMERATA TOP DACTYLIS GLOMERATA TOP AGROSTIS GIGANTEA POLLEN AGROSTIS GIGANTEA POLLEN PHLEUM PRATENSE TOP PHLEUM PRATENSE TOP SOLIDAGO VIRGAUREA FLOWERING TOP SOLIDAGO VIRGAUREA FLOWERING TOP TRIFOLIUM PRATENSE FLOWER TRIFOLIUM PRATENSE FLOWER ALFALFA ALFALFA AMBROSIA TRIFIDA POLLEN AMBROSIA TRIFIDA POLLEN AMBROSIA ACANTHICARPA POLLEN AMBROSIA ACANTHICARPA POLLEN AMBROSIA PSILOSTACHYA POLLEN AMBROSIA PSILOSTACHYA POLLEN ULMUS AMERICANA POLLEN ULMUS AMERICANA POLLEN PLATANUS OCCIDENTALIS POLLEN PLATANUS OCCIDENTALIS POLLEN FRAXINUS AMERICANA POLLEN FRAXINUS AMERICANA POLLEN FAGUS GRANDIFOLIA POLLEN FAGUS GRANDIFOLIA POLLEN JUGLANS NIGRA POLLEN JUGLANS NIGRA POLLEN SALIX NIGRA POLLEN SALIX NIGRA BARK ACER NEGUNDO POLLEN ACER NEGUNDO POLLEN POPULUS DELTOIDES SUBSP. DELTOIDES POLLEN POPULUS DELTOIDES POLLEN BETULA OCCIDENTALIS POLLEN BETULA OCCIDENTALIS POLLEN QUERCUS RUBRA POLLEN QUERCUS RUBRA POLLEN CARYA OVATA POLLEN CARYA OVATA POLLEN SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER HISTAMINE DIHYDROCHLORIDE HISTAMINE ARSENIC TRIOXIDE ARSENIC CATION (3+) PHOSPHORUS PHOSPHORUS PULSATILLA VULGARIS PULSATILLA VULGARIS SULFUR SULFUR WATER ALCOHOL
INDICATIONS: For temporary relief of allergies due to animals. ** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Mammaryplex Echinacea angustifolia, Hydrastis canadensis, Myrrha, Phytolacca decandra, Trigonella foenum-graecum, Lymph, Spleen, Bryonia alba, Bufo rana, Conium maculatum, Lac canium, Lachesis mutus, Silicea, Mammary gland ECHINACEA ANGUSTIFOLIA ECHINACEA ANGUSTIFOLIA GOLDENSEAL GOLDENSEAL MYRRH MYRRH PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT FENUGREEK SEED FENUGREEK SEED SUS SCROFA LYMPH SUS SCROFA LYMPH SUS SCROFA SPLEEN SUS SCROFA SPLEEN BRYONIA ALBA ROOT BRYONIA ALBA ROOT BUFO BUFO CUTANEOUS GLAND BUFO BUFO CUTANEOUS GLAND CONIUM MACULATUM FLOWERING TOP CONIUM MACULATUM FLOWERING TOP CANIS LUPUS FAMILIARIS MILK CANIS LUPUS FAMILIARIS MILK LACHESIS MUTA VENOM LACHESIS MUTA VENOM SILICON DIOXIDE SILICON DIOXIDE SUS SCROFA MAMMA SUS SCROFA MAMMA WATER ALCOHOL
INDICATIONS: For temporary relief of symptoms related to Lyme Disease or other viruses including joint pain, severe headache, fever, severe muscle aches/pain, flu-like feeling of headache, stiff neck, fever, muscle aches, and profound fatigue, circular rash surrounding the site of a tick bite, vision changes and change in smell/taste, difficulty chewing, swallowing, or speaking; hoarseness or vocal cord problems; facial paralysis.
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.
Allergen II Kali gluconicum, Adrenalinum, Hepar (bovinum), Arsenicum album, Phosphorus, Pulsatilla, Sulphur, Histaminum hydrochloricum, Sheep sorrel, Yellow dock, June grass, Orchard grass, Red Top grass, Timorthy grass, Solidago virgaurea, Trifolium pratense, False ragweed, Short ragweed, Tall ragweed, Western ragweed, Ash, Beech, Red Birch, Box Elder, Cottonwood, Elm, Hickory, Red Oak, Sycamore, Blace Walnut, Balce Willow EPINEPHRINE EPINEPHRINE RED CLOVER RED CLOVER ALFALFA ALFALFA ARSENIC TRIOXIDE ARSENIC CATION (3+) PHOSPHORUS PHOSPHORUS PULSATILLA VULGARIS PULSATILLA VULGARIS HISTAMINE DIHYDROCHLORIDE HISTAMINE ALCOHOL SULFUR SULFUR AMBROSIA ARTEMISIIFOLIA AMBROSIA ARTEMISIIFOLIA WATER BEEF LIVER BEEF LIVER RUMEX ACETOSELLA POLLEN RUMEX ACETOSELLA POLLEN RUMEX CRISPUS POLLEN RUMEX CRISPUS POLLEN POA PRATENSIS POLLEN POA PRATENSIS POLLEN DACTYLIS GLOMERATA TOP DACTYLIS GLOMERATA TOP AGROSTIS GIGANTEA TOP AGROSTIS GIGANTEA TOP PHLEUM PRATENSE POLLEN PHLEUM PRATENSE POLLEN SOLIDAGO VIRGAUREA POLLEN SOLIDAGO VIRGAUREA POLLEN AMBROSIA ACANTHICARPA POLLEN AMBROSIA ACANTHICARPA POLLEN AMBROSIA PSILOSTACHYA POLLEN AMBROSIA PSILOSTACHYA POLLEN FRAXINUS AMERICANA POLLEN FRAXINUS AMERICANA POLLEN FAGUS GRANDIFOLIA POLLEN FAGUS GRANDIFOLIA POLLEN BETULA OCCIDENTALIS POLLEN BETULA OCCIDENTALIS POLLEN ACER NEGUNDO POLLEN ACER NEGUNDO POLLEN POPULUS DELTOIDES POLLEN POPULUS DELTOIDES POLLEN ULMUS AMERICANA POLLEN ULMUS AMERICANA POLLEN CARYA CORDIFORMIS POLLEN CARYA CORDIFORMIS POLLEN QUERCUS RUBRA POLLEN QUERCUS RUBRA POLLEN PLATANUS OCCIDENTALIS POLLEN PLATANUS OCCIDENTALIS POLLEN JUGLANS NIGRA POLLEN JUGLANS NIGRA POLLEN SALIX NIGRA POLLEN SALIX NIGRA POLLEN POTASSIUM GLUCONATE POTASSIUM CATION AMBROSIA TRIFIDA POLLEN AMBROSIA TRIFIDA POLLEN KOELERIA MACRANTHA POLLEN KOELERIA MACRANTHA POLLEN