NDC 48951-1037

Antimonite Belladonna

Antimonite Belladonna

Antimonite Belladonna is a Oral Powder in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Antimony Trisulfide; Atropa Belladonna; Matricaria Recutita; Bismuth Subnitrate.

Product ID48951-1037_6983c4f2-0167-ba15-e053-2991aa0a3625
NDC48951-1037
Product TypeHuman Otc Drug
Proprietary NameAntimonite Belladonna
Generic NameAntimonite Belladonna
Dosage FormPowder
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameANTIMONY TRISULFIDE; ATROPA BELLADONNA; MATRICARIA RECUTITA; BISMUTH SUBNITRATE
Active Ingredient Strength3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-1037-4

50 g in 1 BOTTLE, GLASS (48951-1037-4)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-1037-4 [48951103704]

Antimonite Belladonna POWDER
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
ANTIMONY TRISULFIDE3 [hp_X]/g

OpenFDA Data

SPL SET ID:0bc61339-130a-459b-9c61-2a12b5572347
Manufacturer
UNII

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