- Product NDC
- 43742-2222
- 11-digit product format
- 437422222
- Labeler code
- 43742
- Product ID
- 43742-2222_498c0781-09c0-48e6-81d5-f27c998a310c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allium Sativum, Alumina, Antipyrinum, Benzinum, Bisphenol A, Carbolicum Acidum, Carboneum Sulphuratum, Diethylstilbestrol, Dioxin, Folliculinum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Paraffinum, Petroleum, Phenacetinum, Ptelea Trifoliata, Sodium Carboxymethyl Cellulose, Teflon
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-12-13
- Substance
- 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN; ALUMINUM OXIDE; ANTIPYRINE; BENZENE; BISPHENOL A; CARBON DISULFIDE; CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED; DIETHYLSTILBESTROL; ESTRONE; FORMALDEHYDE SOLUTION; GARLIC; GLYPHOSATE; KEROSENE; METHYLPARABEN; NAPHTHALENE; PARAFFIN; PHENACETIN; PHENOL; POLYTETRAFLUOROETHYLENE; PTELEA TRIFOLIATA BARK
- Active strength
- 36; 12; 18; 12; 12; 9; 12; 15; 12; 12; 6; 12; 8; 12; 12; 12; 14; 12; 33; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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_C]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes