HF ACQUISITION CO. LLC, DBA HEALTH FIRST
FDA
Rx Only
25% Dextrose Injection, USP is a sterile, nonpyrogenic, hypertonic solution of dextrose in water for injection administered by intravenous injection to restore blood glucose levels in hypoglycemia and as a source of carbohydrate calories. Each milliliter (mL) of fluid contains dextrose, hydrous, 250 mg which delivers 3.4 kcal/gram (0.85 kcal/mL). The solution has an osmolarity of 1.39 mOsmol/mL (calc.). pH is 4.5 (3.2 to 6.5). May contain hydrochloric acid and sodium hydroxide for pH adjustment. The solution contains no bacteriostat, antimicrobial agent or added buffer (except for pH adjustment) and is intended only for use as a single-dose injection. When smaller doses are required the unused portion should be discarded with the entire unit. 25% Dextrose Injection, USP is a dextrose (glucose) and nutrient (carbohydrate) replenisher. Dextrose, USP is chemically designated D-glucose monohydrate, (C6H12O6 • H2O), a hexose sugar freely soluble in water. It has the following structural formula: The syringe is molded from a specially formulated polypropylene. Water permeates from inside the container at an extremely slow rate which will have an insignificant effect on solution concentration over the expected shelf life. 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 syringe material. Dextrose Structure
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.
HF ACQUISITION CO LLC, DBA HEALTHFIRST
FDA
Rx Only
50% Dextrose Injection, USP is a sterile, nonpyrogenic, hypertonic solution of dextrose in water for injection for intravenous injection as a fluid and nutrient replenisher. Each mL of fluid contains 0.5 g dextrose, hydrous which delivers 3.4 kcal/gram. The solution has an osmolarity of 2.53 mOsmol/mL (calc.), a pH of 4.2 (3.2 to 6.5) and may contain sodium hydroxide and/or hydrochloric acid for pH adjustment. The solution contains no bacteriostat, antimicrobial agent or added buffer (except for pH adjustment) and is intended only for use as a single-dose injection. When smaller doses are required, the unused portion should be discarded with the entire unit. Dextrose, USP is chemically designated C6H12O6 ∙ H2O (D-glucose monohydrate), a hexose sugar freely soluble in water. Dextrose, hydrous has the following structural formula: Water for Injection, USP is chemically designated H2O. The syringe is molded from a specially formulated polypropylene. Water permeates from inside the container at an extremely slow rate which will have an insignificant effect on solution concentration over the expected shelf life. 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 syringe material. STRUCTURE
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.
Uses: For temporary relief of minor: fatigue* irritability* cramps* exhaustion* restlessness* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Uses: For temporary relief of minor: spasms* fatigue* headache* congestion* dry skin* nervous irritability* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Uses: For temporary relief of minor: rash* sore throat* constipation* headache* coughing* muscle soreness* swollen ankle* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Sterile. Non-pyrogenic. Do not use unless the solution is clear and the container is intact. Rx Only. Single use container. For use only with apheresis devices. See apheresis device operator's manual for complete instructions.
ACD ACITRIC ACID MONOHYDRATE DEXTROSE MONOHYDRATE AND TRISODIUM CITRATE DIHYDRATE
ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is designed to be metered by an apheresis device in apheresis procedures, to prevent platelet activation and coagulation as blood moves throughout the extracorporeal unit (tubing set) in an apheresis procedure. The solution is sterile and non-pyrogenic, and it contains no bacteriostatic or antimicrobial agents. The formulas of the active ingredients are provided in Table 1. Table 1: Active Ingredients Ingredients Molecular Formula Molecular Weight (%w/v) Citric Acid, Monohydrate C 6 H 8 O 7 192.12 Dextrose Monohydrate C 6 H 12 O 6 ∙ H 2 O 198.17 Sodium Citrate Dihydrate C 6 H 9 Na 3 O 9 294.10 Water for Injection H 2 O 18.00 Each 100 mL of ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A contains: (%w/v) Citric Acid, Monohydrate 0.8 g; Dextrose Monohydrate 2.45 g; Sodium Citrate Dihydrate 2.2 g; and Water for Injection. The polyolefin bag is not made with natural rubber latex or PVC. The bag is made from a multilayered film. It contains materials that have been tested to demonstrate the suitability of the container for storing pharmaceutical solutions. The solution contact layer is an elasticized polyolefin. The bag is nontoxic and biologically inert. The bag-solution unit is a closed system and is not dependent upon entry of external air during administration. The bag is overwrapped to provide protection from the physical environment and to provide an additional moisture barrier when necessary.
INDICATIONS & USAGE SECTION Aches - Pains: Formulated for symptoms associated with bruises, strains and overexertion such as pain, stiffness and inflammation.
INDICATIONS & USAGE SECTION Aches - Pains Formulated for symptoms associated with bruises, strains and overexertion such as pain, stiffness and inflammation.
Indications & Usage: Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue before meals or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.
Uses temporarily relieves symptoms contributing to: excessive appetite, constitutional tndency to gain fat, overeating, cravings for sweets and starches, water retention, excess weight, abdominal fat.
Endopath-F Homeopathic Liquid CHASTE TREE CHASTE TREE BLACK COHOSH BLACK COHOSH FUCUS VESICULOSUS FUCUS VESICULOSUS GLYCYRRHIZA GLABRA GLYCYRRHIZA GLABRA BOS TAURUS HYPOTHALAMUS BOS TAURUS HYPOTHALAMUS ANGELICA SINENSIS ROOT ANGELICA SINENSIS ROOT SUS SCROFA OVARY SUS SCROFA OVARY PULSATILLA VULGARIS PULSATILLA VULGARIS SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE THYROID, UNSPECIFIED THYROID, UNSPECIFIED ZANTHOXYLUM AMERICANUM BARK ZANTHOXYLUM AMERICANUM BARK SUS SCROFA PITUITARY GLAND SUS SCROFA PITUITARY GLAND SUS SCROFA ADRENAL GLAND SUS SCROFA ADRENAL GLAND WATER GLYCERIN ALCOHOL
INDICATIONS: For temporary relief of symptoms related to food additives, herbicides and insecticides including muscle weakness, skin irritations, poor muscle coordination, headache, cough, diarrhea, dizziness, fatigue, fever, pneumonia, stomach pain and vomiting.
INDICATIONS: For temporary relief of symptoms including arrhythmia, anxiety, depression, headache, reading difficulty, trembling of limbs, and poor memory.
INDICATIONS: For temporary relief of symptoms related to gastroenteritis including diarrhea, stomach cramps, nausea, vomiting, fluid and electrolyte depletion, flatulence and bloating.
HOMEOPATHIC INDICATIONS: For temporary reduction of the symptoms of insomnia.** **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 of itching, tingling, burning, or painful feeling along with a painful rash.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INDICATIONS: For temporary relief of symptoms related to heavy metal toxicity including gastritis, cough, poor concentration, nausea, vomiting, diarrhea, stomach pain, sweating, and a metallic taste in the mouth.
Acetaldehyde Acetaldehyde ACETALDEHYDE ACETALDEHYDE WATER ALCOHOL
HOMEOPATHIC INDICATIONS: For temporary relief of symptoms caused by sensitivities to perfumes, flavors, dyes, plastics, alcohol or foods including sneezing, headache, bronchitis, difficult breathing, and digestive malfunction.** **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.