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Skin Tag Remover - 57955-7800-3 - (Thuja occidentalis)

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Drug Information of Skin Tag Remover

Product NDC: 57955-7800
Proprietary Name: Skin Tag Remover
Non Proprietary Name: Thuja occidentalis
Active Ingredient(s): 6    [hp_X]/15mL & nbsp;   Thuja occidentalis
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Skin Tag Remover

Product NDC: 57955-7800
Labeler Name: King Bio Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130426

Package Information of Skin Tag Remover

Package NDC: 57955-7800-3
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON (57955-7800-3) > 15 mL in 1 BOTTLE, WITH APPLICATOR

NDC Information of Skin Tag Remover

NDC Code 57955-7800-3
Proprietary Name Skin Tag Remover
Package Description 1 BOTTLE, WITH APPLICATOR in 1 CARTON (57955-7800-3) > 15 mL in 1 BOTTLE, WITH APPLICATOR
Product NDC 57955-7800
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Thuja occidentalis
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20130426
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name King Bio Inc.
Substance Name THUJA OCCIDENTALIS LEAFY TWIG
Strength Number 6
Strength Unit [hp_X]/15mL
Pharmaceutical Classes

Complete Information of Skin Tag Remover


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