NDC 48951-4009

Drosera comp.

Drosera Comp.

Drosera comp. is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Drosera Rotundifolia; Atropa Belladonna; Quillaja Saponaria Bark; Protortonia Cacti; Helleborus Foetidus Root; Ipecac; Mephitis Mephitis Anal Gland Fluid; Veratrum Album Root.

Product ID48951-4009_6aaf20bc-356c-4851-e053-2a91aa0a56a8
NDC48951-4009
Product TypeHuman Otc Drug
Proprietary NameDrosera comp.
Generic NameDrosera Comp.
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameDROSERA ROTUNDIFOLIA; ATROPA BELLADONNA; QUILLAJA SAPONARIA BARK; PROTORTONIA CACTI; HELLEBORUS FOETIDUS ROOT; IPECAC; MEPHITIS MEPHITIS ANAL GLAND FLUID; VERATRUM ALBUM ROOT
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
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-4009-3

60 mL in 1 BOTTLE, DROPPER (48951-4009-3)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-4009-3 [48951400903]

Drosera comp. LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
DROSERA ROTUNDIFOLIA3 [hp_X]/mL

OpenFDA Data

SPL SET ID:cfb0332c-1a02-4f0a-9f5d-0bbae4fa3af2
Manufacturer
UNII

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