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Dairy Allergen Mix

Wirkstoff: ADENOSINE TRIPHOSPHATE DISODIUM, BENZOIC ACID, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, TRIBASIC CALCIUM PHOSPHATE, CALCIUM CITRATE, CALCIUM GLUCONATE, ACTIVATED CHARCOAL, MATRICARIA CHAMOMILLA WHOLE, CHOLINE HYDROXIDE, CINNAMIC ACID, COUMARIN, EUGENOL, FOLIC ACID, ESTRONE, FORMALDEHYDE SOLUTION, .GAMMA.-AMINOBUTYRIC ACID, SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS, HISTAMINE DIHYDROCHLORIDE, SUS SCROFA ILEUM, SUS SCROFA JEJUNUM, ASPARAGINE MONOHYDRATE, CANIS LUPUS FAMILIARIS MILK, SKIM MILK, FELIS CATUS MILK, HUMAN MILK, COW MILK, MENADIONE, SUS SCROFA OVARY, PETROSELINUM CRISPUM WHOLE, PHENYL ISOTHIOCYANATE, PIPERINE, QUERCETIN, TOXICODENDRON PUBESCENS LEAF, RUTIN, LACTOSE, UNSPECIFIED FORM, LACTIC ACID, L-, SUS SCROFA STOMACH

Flüssigkeit [Übersetzung der Form; Original: LIQUID (openFDA)] · ADENOSINE TRIPHOSPHATE DISODIUM 4 [hp_X]/mL, BENZOIC ACID 6 [hp_X]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_C]/mL, CALCIUM FLUORIDE 6 [hp_C]/mL, TRIBASIC CALCIUM PHOSPHATE 6 [hp_C]/mL, CALCIUM CITRATE 6 [hp_C]/mL, CALCIUM GLUCONATE 6 [hp_C]/mL, ACTIVATED CHARCOAL 6 [hp_C]/mL, MATRICARIA CHAMOMILLA WHOLE 6 [hp_C]/mL, CHOLINE HYDROXIDE 6 [hp_X]/mL, CINNAMIC ACID 6 [hp_X]/mL, COUMARIN 8 [hp_X]/mL, EUGENOL 6 [hp_X]/mL, FOLIC ACID 6 [hp_X]/mL, ESTRONE 8 [hp_X]/mL, FORMALDEHYDE SOLUTION 6 [hp_X]/mL, .GAMMA.-AMINOBUTYRIC ACID 8 [hp_X]/mL, SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS 12 [hp_C]/mL, HISTAMINE DIHYDROCHLORIDE 6 [hp_X]/mL, SUS SCROFA ILEUM 8 [hp_X]/mL, SUS SCROFA JEJUNUM 8 [hp_X]/mL, ASPARAGINE MONOHYDRATE 6 [hp_X]/mL, CANIS LUPUS FAMILIARIS MILK 30 [hp_X]/mL, SKIM MILK 6 [hp_X]/mL, FELIS CATUS MILK 30 [hp_X]/mL, HUMAN MILK 30 [hp_X]/mL, COW MILK 6 [hp_X]/mL, MENADIONE 6 [hp_X]/mL, SUS SCROFA OVARY 6 [hp_X]/mL, PETROSELINUM CRISPUM WHOLE 6 [hp_X]/mL, PHENYL ISOTHIOCYANATE 6 [hp_X]/mL, PIPERINE 30 [hp_X]/mL, QUERCETIN 6 [hp_X]/mL, TOXICODENDRON PUBESCENS LEAF 6 [hp_C]/mL, RUTIN 6 [hp_C]/mL, LACTOSE, UNSPECIFIED FORM 6 [hp_X]/mL, LACTIC ACID, L- 8 [hp_X]/mL, SUS SCROFA STOMACH 8 [hp_X]/mL

Vereinigte StaatenAktiv

Zulassungsinhaber: Deseret Biologicals, Inc.

Geprüft 2026-10-09 · openFDA NDC

Zusammensetzung
Zulassung
Zulassungsnummer
43742-2201
Zulassungsstatus
Aktiv
Abgabe
Rezeptfrei
Art der Anwendung
ORAL
Quellen