- Product NDC
- 44911-0725
- 11-digit product format
- 449110725
- Labeler code
- 44911
- Product ID
- 44911-0725_037a3c93-3157-4424-a28d-b8445eb46d6e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Butyl Acetate, Ethyl Acetate, Toluene, Xylene, Bisphenol A, Petroleum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Propylparaben, Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla (Pratensis), Sulphur, Paraffinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-12-20
- Substance
- ACETONE; AMMONIUM CHLORIDE; BENZENE; BISPHENOL A; BUTYL ACETATE; ETHYL ACETATE; FORMALDEHYDE SOLUTION; GLYPHOSATE; GRAPHITE; KEROSENE; METHYLPARABEN; NAPHTHALENE; NITRIC ACID; PARAFFIN; PROPYLENE GLYCOL; PROPYLPARABEN; PULSATILLA PRATENSIS WHOLE; SEMECARPUS ANACARDIUM JUICE; SODIUM LAURYL SULFATE; SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM; SULFUR; TOLUENE; TURPENTINE OIL; XYLENE (MIXED ISOMERS)
- Active strength
- 9; 9; 9; 9; 9; 9; 9; 9; 12; 9; 9; 9; 12; 12; 9; 9; 12; 12; 9; 9; 12; 9; 9; 9 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes