Dairy Allergen Mix

Product NDC
43742-1277
11-digit product format
437421277
Labeler code
43742
Product ID
43742-1277_8e05dfed-90b2-4f6f-a616-da89d64a1c7e
Type
HUMAN OTC DRUG
Nonproprietary name
Adenosinum Triphosphoricum Dinatrum, Apiolum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Eugenol, Folic Acid, Formalinum, Histaminum Hydrochloricum, L-Asparagine (Monohydrate), Lac Defloratum, Lac Vaccinum, Menadione, Oophorinum (Suis), Phenyl Isothiocyanate, Quercetin, Rutin, Saccharum Lactis, Ileum (Suis), Jejunum (Suis), Stomach (Suis), Coumarinum, Folliculinum, GABA (Gamma-Aminobutyric Acid), Sarcolacticum Acidum, Lac Caninum, Lac Felinum, Lac Humanum, Piperine, Calcarea Carbonica, Calcarea Fluorica,
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2018-12-31
Marketing end
2025-02-17
Substance
ADENOSINE TRIPHOSPHATE DISODIUM; APIOLE (PARSLEY); BENZOIC ACID; CHOLINE HYDROXIDE; CINNAMIC ACID; EUGENOL; FOLIC ACID; FORMALDEHYDE; HISTAMINE DIHYDROCHLORIDE; ASPARAGINE MONOHYDRATE; SKIM MILK; COW MILK; MENADIONE; SUS SCROFA OVARY; PHENYL ISOTHIOCYANATE; QUERCETIN; RUTIN; LACTOSE, UNSPECIFIED FORM; SUS SCROFA ILEUM; SUS SCROFA JEJUNUM; SUS SCROFA STOMACH; COUMARIN; ESTRONE; .GAMMA.-AMINOBUTYRIC ACID; LACTIC ACID, L-; CANIS LUPUS FAMILIARIS MILK; FELIS CATUS MILK; HUMAN MILK; PIPERINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; ACTIVATED CHARCOAL; MATRICARIA RECUTITA; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; TOXICODENDRON PUBESCENS LEAF; CALCIUM CITRATE; CALCIUM GLUCONATE
Active strength
4 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1277-14374212770130 mL in 1 BOTTLE, DROPPER (43742-1277-1) 30 ml2018-12-312025-02-17NoNoCurrent