Label: TAG AWAY- thuja occidentalis liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 65121-623-10 - Packager: Pure Source
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated January 2, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Warnings:
- Directions:
- Active Ingredients:
- Inactive Ingredients:
- Purpose:
- Keep out of reach of children.
- Directions:
- Tag Away Skin Tag Remover
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INGREDIENTS AND APPEARANCE
TAG AWAY
thuja occidentalis liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65121-623 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength THUJA OCCIDENTALIS BARK (UNII: 19RAD88E6O) (THUJA OCCIDENTALIS BARK - UNII:19RAD88E6O) THUJA OCCIDENTALIS BARK 6 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength CEDAR LEAF OIL (UNII: BJ169U4NLG) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) RICINUS COMMUNIS SEED (UNII: 7EK4SFN1TX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65121-623-10 10 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/04/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/18/2012 Labeler - Pure Source (080354456) Establishment Name Address ID/FEI Business Operations Pure Source 080354456 manufacture(65121-623)