NDC 48951-2115

Berberis Prunus

Berberis Prunus

Berberis Prunus is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Sloe; Berberis Vulgaris Root Bark; Lemon; Quince.

Product ID48951-2115_6a857887-8cc4-f1a9-e053-2991aa0af37d
NDC48951-2115
Product TypeHuman Otc Drug
Proprietary NameBerberis Prunus
Generic NameBerberis Prunus
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameSLOE; BERBERIS VULGARIS ROOT BARK; LEMON; QUINCE
Active Ingredient Strength1 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 48951-2115-5

1 TUBE in 1 BAG (48951-2115-5) > 10 g in 1 TUBE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-2115-5 [48951211505]

Berberis Prunus OINTMENT
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

NDC 48951-2115-1 [48951211501]

Berberis Prunus OINTMENT
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01
Marketing End Date2019-06-12

Drug Details

Active Ingredients

IngredientStrength
SLOE1 [hp_X]/g

OpenFDA Data

SPL SET ID:8d01ba95-2c9e-4732-9937-070b9e543789
Manufacturer
UNII

NDC Crossover Matching brand name "Berberis Prunus" or generic name "Berberis Prunus"

NDCBrand NameGeneric Name
48951-2049Berberis PrunusBerberis Prunus
48951-2050Berberis PrunusBerberis Prunus
48951-2115Berberis PrunusBerberis Prunus
48951-2140Berberis PrunusBerberis Prunus
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