NDC 48951-3091

Cichorium Oxalis

Cichorium Oxalis

Cichorium Oxalis is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Cichorium Intybus Whole; Oxalis Acetosella Leaf; Activated Charcoal; Sus Scrofa Pancreas; Barium Citrate; Iron.

Product ID48951-3091_559efa5b-91c5-2b52-e054-00144ff88e88
NDC48951-3091
Product TypeHuman Otc Drug
Proprietary NameCichorium Oxalis
Generic NameCichorium Oxalis
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameCICHORIUM INTYBUS WHOLE; OXALIS ACETOSELLA LEAF; ACTIVATED CHARCOAL; SUS SCROFA PANCREAS; BARIUM CITRATE; IRON
Active Ingredient Strength3 [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 48951-3091-1

10 AMPULE in 1 BOX (48951-3091-1) > 1 mL in 1 AMPULE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-3091-1 [48951309101]

Cichorium Oxalis LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
CICHORIUM INTYBUS WHOLE3 [hp_X]/mL

OpenFDA Data

SPL SET ID:3d284b66-6a25-4d6f-9d37-e7642ae88d3b
Manufacturer
UNII

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