NDC 48951-1114

Arnica Betula A

Arnica Betula A

Arnica Betula A is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Betula Pubescens Leaf; Betula Pubescens Bark; Bos Taurus Cerebellum; Bos Taurus Brain; Bos Taurus Pituitary Gland; Bos Taurus Eye; Bos Taurus Nerve; Sus Scrofa Thalamus; Arnica Montana; Silicon Dioxide; Honey; Lead.

Product ID48951-1114_6c7bf5ba-9649-d668-e053-2991aa0af4e6
NDC48951-1114
Product TypeHuman Otc Drug
Proprietary NameArnica Betula A
Generic NameArnica Betula A
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameBETULA PUBESCENS LEAF; BETULA PUBESCENS BARK; BOS TAURUS CEREBELLUM; BOS TAURUS BRAIN; BOS TAURUS PITUITARY GLAND; BOS TAURUS EYE; BOS TAURUS NERVE; SUS SCROFA THALAMUS; ARNICA MONTANA; SILICON DIOXIDE; HONEY; LEAD
Active Ingredient Strength3 [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
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-1114-1

10 AMPULE in 1 BOX (48951-1114-1) > 1 mL in 1 AMPULE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-1114-1 [48951111401]

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

Drug Details

Active Ingredients

IngredientStrength
BETULA PUBESCENS LEAF3 [hp_X]/mL

OpenFDA Data

SPL SET ID:6c0ef994-f548-4052-bf2c-9d02badb99a4
Manufacturer
UNII

NDC Crossover Matching brand name "Arnica Betula A" or generic name "Arnica Betula A"

NDCBrand NameGeneric Name
48951-1114Arnica Betula AArnica Betula A
48951-1115Arnica Betula AArnica Betula A
48951-1352Arnica Betula AArnica Betula A

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.