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Skin Tag Relief - 68229-100-02 - (Thuja Occidentalis Leafy Twig)

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Drug Information of Skin Tag Relief

Product NDC: 68229-100
Proprietary Name: Skin Tag Relief
Non Proprietary Name: Thuja Occidentalis Leafy Twig
Active Ingredient(s): 6    [hp_X]/10mL & nbsp;   Thuja Occidentalis Leafy Twig
Administration Route(s): TOPICAL
Dosage Form(s): OIL
Coding System: National Drug Codes(NDC)

Labeler Information of Skin Tag Relief

Product NDC: 68229-100
Labeler Name: Quest Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130521

Package Information of Skin Tag Relief

Package NDC: 68229-100-02
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-02) > 10 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-01)

NDC Information of Skin Tag Relief

NDC Code 68229-100-02
Proprietary Name Skin Tag Relief
Package Description 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-02) > 10 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-01)
Product NDC 68229-100
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Thuja Occidentalis Leafy Twig
Dosage Form Name OIL
Route Name TOPICAL
Start Marketing Date 20130521
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Quest Products, Inc.
Substance Name THUJA OCCIDENTALIS LEAFY TWIG
Strength Number 6
Strength Unit [hp_X]/10mL
Pharmaceutical Classes

Complete Information of Skin Tag Relief


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