Dairy Allergen Mix
- Product NDC
- 43742-0579
- 11-digit product format
- 437420579
- Labeler code
- 43742
- Product ID
- 43742-0579_edc02db5-656e-41d3-8589-0606cc92c4c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adenosinum Triphosphoricum Dinatrum, Apiolum, Benzoicum Acidum, Cholinum, Cinnamic Acid, Coumarinum, Eugenol, Folic Acid, Folliculinum, Formalinum, GABA (Gamma-Aminobutyric Acid), Histaminum Hydrochloricum, L-Asparagine (Monohydrate), Lac Defloratum, Lac Vaccinum, Menadione, Oophorinum (Suis), Phenyl Isothiocyanate, Quercetin, Rutin, Saccharum Lactis, Ileum (Suis), Jejunum (Suis), Stomach (Suis), Sarcolacticum Acidum, Lac Caninum, Lac Felinum, Lac Humanum, Piperine, Calcarea Carbonica
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-05-07
- Marketing end
- 2023-06-12
- Substance
- ADENOSINE TRIPHOSPHATE DISODIUM; APIOLE (PARSLEY); BENZOIC ACID; CHOLINE HYDROXIDE; CINNAMIC ACID; COUMARIN; EUGENOL; FOLIC ACID; ESTRONE; FORMALDEHYDE; .GAMMA.-AMINOBUTYRIC ACID; HISTAMINE DIHYDROCHLORIDE; ASPARAGINE MONOHYDRATE; SKIM MILK; COW MILK; MENADIONE; SUS SCROFA OVARY; PHENYL ISOTHIOCYANATE; QUERCETIN; RUTIN; LACTOSE; SUS SCROFA ILEUM; SUS SCROFA JEJUNUM; SUS SCROFA STOMACH; 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_X]/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 NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0579-1 | 43742057901 | 30 mL in 1 BOTTLE, DROPPER (43742-0579-1) | 30 ml | 2015-05-07 | 2023-06-12 | No | No | Current |