NDC 48951-1155

Arnica Scorodite

Arnica Scorodite

Arnica Scorodite is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Silicon Dioxide; Arnica Montana; Ostrea Edulis Shell; Levisticum Officinale Root; Sodium Carbonate; Orchis Mascula Tuber; Fluorapatite; Ferrous Arsenate; Bos Taurus Cerebellum.

Product ID48951-1155_6c7b93ca-ee8e-3c2e-e053-2a91aa0ad23e
NDC48951-1155
Product TypeHuman Otc Drug
Proprietary NameArnica Scorodite
Generic NameArnica Scorodite
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameSILICON DIOXIDE; ARNICA MONTANA; OSTREA EDULIS SHELL; LEVISTICUM OFFICINALE ROOT; SODIUM CARBONATE; ORCHIS MASCULA TUBER; FLUORAPATITE; FERROUS ARSENATE; BOS TAURUS CEREBELLUM
Active Ingredient Strength6 [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
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-1155-1

10 AMPULE in 1 BOX (48951-1155-1) > 1 mL in 1 AMPULE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-1155-1 [48951115501]

Arnica Scorodite LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
SILICON DIOXIDE6 [hp_X]/mL

OpenFDA Data

SPL SET ID:b37085ad-74f7-4cf7-b2bb-dd15c842b9b4
Manufacturer
UNII

NDC Crossover Matching brand name "Arnica Scorodite" or generic name "Arnica Scorodite"

NDCBrand NameGeneric Name
48951-1155Arnica ScoroditeArnica Scorodite
48951-1156Arnica ScoroditeArnica Scorodite

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