AVENA DNA ELAEIS GLANDULA SUPRARENALIS SUIS HAMAMELIS HEPAR SUIS KALI SULPH NAT MUR NICOTINAMIDUM PHOSPHORICUM AC PITUITARUM POSTERIUM RIBOFLAVINUM THIAMINUM HYDROCHLORICUM THUJA OCC THYROIDINUM URTICA UR.
Related medications based on brand, generic name, substance, active ingredients.
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
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 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
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.
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 IN LOOK Ginseng Anit wrink Anti wrinkle essenceNIACINAMIDE
Effect: with a refreshing andradiant texture,it has a delicatetouch thatiseasy toandst oothabsorb .ltreplenishesthenecessanmoistureandnutrients for the skin,improvesdryness ,wrinkles and firming.reduces fine lines,providesintensivecare,lifts and solidifiesthe skin leaving it soft,smooth.and radiant with youthfulradiance
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
By Active Ingredients
Drugs sharing any active ingredients
Spine and Nerve Balance Core Formula Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-Lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (Suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis BERBERIS VULGARIS ROOT BARK BERBERIS VULGARIS ROOT BARK BLACK COHOSH BLACK COHOSH CINCHONA OFFICINALIS BARK CINCHONA OFFICINALIS BARK CITRULLUS COLOCYNTHIS FRUIT PULP CITRULLUS COLOCYNTHIS FRUIT PULP LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG RANUNCULUS BULBOSUS RANUNCULUS BULBOSUS HORSE CHESTNUT HORSE CHESTNUT CUPRIC ACETATE CUPRIC CATION NADIDE NADIDE SODIUM DIETHYL OXALACETATE DIETHYL OXALACETATE NIACINAMIDE NIACINAMIDE PICRIC ACID PICRIC ACID PYRIDOXINE HYDROCHLORIDE PYRIDOXINE RIBOFLAVIN RIBOFLAVIN THIAMINE HYDROCHLORIDE THIAMINE ION .ALPHA.-LIPOIC ACID .ALPHA.-LIPOIC ACID AMMONIUM CHLORIDE AMMONIUM CATION SUS SCROFA CARTILAGE SUS SCROFA CARTILAGE SUS SCROFA INTERVERTEBRAL DISC SUS SCROFA INTERVERTEBRAL DISC SILICON DIOXIDE SILICON DIOXIDE SILVER SILVER TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION COENZYME A COENZYME A SUS SCROFA UMBILICAL CORD SUS SCROFA UMBILICAL CORD SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PSEUDOGNAPHALIUM OBTUSIFOLIUM PSEUDOGNAPHALIUM OBTUSIFOLIUM SUS SCROFA BONE MARROW SUS SCROFA BONE MARROW MERCURIC OXIDE MERCURIC OXIDE SULFUR SULFUR ENTEROBACTER CLOACAE ENTEROBACTER CLOACAE SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS PROTEUS MORGANII PROTEUS MORGANII PROTEUS VULGARIS PROTEUS VULGARIS WATER ALCOHOL
INDICATIONS: Temporary relief of symptoms related to a blocked spine including spasm, pain, anxiety, nervousness and the inability to hold chiropractic spinal adjustments.
USES: Provides scientifically proven support for temporary relief from many issues experienced by those who want to increase muscle mass and enhance recuperation. Benefits may include: - Decreased Bodyfat - More Energy - Increased Muscle Tone - Better Sleep - Improved Strength - Improved Circulation - Enhanced Sex Drive & Performance - Improved Skin Texture, Tone & Elasticity
INDICATIONS: Liver, Gallbladder support.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Temporarily relieves the common symptoms of a reducing diet, including: ° excessive appetite ° food cravings ° low energy ° water retention ° natural ° gluten & lactose free ° no artificial flavors or colors ° no known negative side effects ° no known negative drug interactions
Optimal HCG Fucus vesiculosus, Cyanocobalamin, Glandula suprarenalis suis, Hepar suis, L-carnitine, Ornithine, Antimonium crudum, FUCUS VESICULOSUS FUCUS VESICULOSUS CYANOCOBALAMIN CYANOCOBALAMIN SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND PORK LIVER PORK LIVER LEVOCARNITINE LEVOCARNITINE ORNITHINE ORNITHINE ANTIMONY TRISULFIDE ANTIMONY HUMAN CHORIONIC GONADOTROPIN HUMAN CHORIONIC GONADOTROPIN SUS SCROFA THYROID SUS SCROFA THYROID SODIUM SULFATE SODIUM CATION OYSTER SHELL CALCIUM CARBONATE, CRUDE OYSTER SHELL CALCIUM CARBONATE, CRUDE PANCRELIPASE PANCRELIPASE SUS SCROFA HYPOTHALAMUS SUS SCROFA HYPOTHALAMUS GREEN TEA LEAF ILEX PARAGUARIENSIS LEAF PAULLINIA CUPANA SEED WATER ALCOHOL WITHANIA SOMNIFERA ROOT
USES: Provides scientifically proven support for relief from many issues experienced by those who want to increase muscle mass and enhance recuperation. Benefits may include: *decreased bodyfat *more energy *increased muscle tone *better sleep *improved strength *improved circulation *enhanced sex drive and performance *improves skin texture, tone and elasticity
Weight Loss Solution Amino acids, Apis mellifica, Arnica montana, Fucus vesiculosus, Gambogia, Hepar suis, Phosphoricum acidum Pituitary suis, AMINO ACIDS AMINO ACIDS APIS MELLIFERA APIS MELLIFERA ARNICA MONTANA ARNICA MONTANA FUCUS VESICULOSUS FUCUS VESICULOSUS GAMBOGE GAMBOGE PORK LIVER PORK LIVER PHOSPHORIC ACID PHOSPHORIC ACID SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG SUS SCROFA THYROID SUS SCROFA THYROID WATER ALCOHOL
USES: Provides scientifically proven, multi-angular support for relief from many issues experienced by those who want to lose weight and cut bodyfat. Benefits may include: *support thyroid function *decreased bodyfat *enhanced metabolism *increased muscle tone *more energy *reduced food and carbohydrate cravings *improved digestion and protein synthesis *reduced excess fluid retention.
INDICATIONS: For the temporary relief of symptoms of chronic illness including fatigue, effects of toxin buildup, slowed metabolism, and weakened constitution.
Sprayology Life Detoxer Carduus marianus, Hepar suis, Mercurius solubilis, Mucosa nasalis suis, Plumbum metallicum MILK THISTLE MILK THISTLE PORK LIVER PORK LIVER MERCURIUS SOLUBILIS MERCURIUS SOLUBILIS SUS SCROFA NASAL MUCOSA SUS SCROFA NASAL MUCOSA LEAD LEAD GLYCERIN ALCOHOL WATER
Relieves common symptoms of exposure to indoor and outdoor environmental toxins (including second-hand smoke), such as: ° respiratory difficulties ° coughing ° lung and liver toxicity ° sluggishness ° natural ° gluten free ° no artificial flavors or colors ° no known negative side effects ° no known negative drug interactions
INDICATIONS: For temporary relief of symptoms related to high blood sugar including dry mouth, thirst, excess urination, night sweats, sugar and carb cravings.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Vital HGH Skin, Hair and Nails Amino acids, Apis mellifica, Biotin, Epidermis, Galium aparine, Hamamelis virginiana, Hepar suis, HGH, Natrum muriaticum, AMINO ACIDS AMINO ACIDS APIS MELLIFERA APIS MELLIFERA BIOTIN BIOTIN SUS SCROFA SKIN SUS SCROFA SKIN GALIUM APARINE GALIUM APARINE HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK PORK LIVER PORK LIVER SOMATROPIN SOMATROPIN SODIUM CHLORIDE SODIUM CATION PANTOTHENIC ACID PANTOTHENIC ACID PHOSPHORIC ACID PHOSPHORIC ACID SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND RIBOFLAVIN RIBOFLAVIN THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG WATER ALCOHOL
USES: Revitalizes hair, dry skin and nail growth and helps relieve: *dry, aging skin *brittle nails *slow hair and hail growth *skin blemishes and rashes
Indications : Detoxifies the lungs from inhaled indoor and outdoor pollutants and relieves associated symptoms: shortness of breath, wheezing, coughing, lack of energy. Homeopathic. Doctor formulated. Readily absorbed, safe, no known side effects, easy to use.
INDICATIONS: Phenolic sensitivity.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
HOMEOPATHIC INDICATIONS: For the temporary relief of exhaustion, fatigue, and feelings of low energy.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.