NDC 62795-1016

BHI Skin

Berberis Vulgaris Root Bark, Graphite, Hydrofluoric Acid, Lycopodium Clavatum Spore, Petrolatum, Toxicodendron Pubescens Leaf, Sepia Officinalis Juice, And Sulfur

BHI Skin is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Medinatura Inc. The primary component is Berberis Vulgaris Root Bark; Graphite; Hydrofluoric Acid; Lycopodium Clavatum Spore; Petrolatum; Sepia Officinalis Juice; Sulfur; Toxicodendron Pubescens Leaf.

Product ID62795-1016_29e7a2ad-a3bb-4527-a81d-0c6b4dba65a5
NDC62795-1016
Product TypeHuman Otc Drug
Proprietary NameBHI Skin
Generic NameBerberis Vulgaris Root Bark, Graphite, Hydrofluoric Acid, Lycopodium Clavatum Spore, Petrolatum, Toxicodendron Pubescens Leaf, Sepia Officinalis Juice, And Sulfur
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameMediNatura Inc
Substance NameBERBERIS VULGARIS ROOT BARK; GRAPHITE; HYDROFLUORIC ACID; LYCOPODIUM CLAVATUM SPORE; PETROLATUM; SEPIA OFFICINALIS JUICE; SULFUR; TOXICODENDRON PUBESCENS LEAF
Active Ingredient Strength6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 62795-1016-3

1 PACKAGE in 1 CARTON (62795-1016-3) > 100 TABLET in 1 PACKAGE
Marketing Start Date2015-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62795-1016-2 [62795101602]

BHI Skin TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2015-01-01

Drug Details

Active Ingredients

IngredientStrength
BERBERIS VULGARIS ROOT BARK6 [hp_X]/1
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.