Household Antigens

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