Label: TN DICKINSONS WITCH HAZEL ANTIBACTERIAL- benzethonium chloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 52651-006-01 - Packager: Dickinson Brands Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 9, 2012
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Uses
- Warnings:
- DO NOT USE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions:
- Inactive ingredients:
- QUESTIONS
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Product Packaging
The labels shown below represent a sample of that currently in use. Additional packaging may also be available.
Kills 99.9% of Germs
T.N. DICKINSON'S Witch hazel
Anti-Bacterial Spray
Fast Acting
MAXIMUM STRENGTH
Antiseptic Formula
Benzethonium Chloride 0.2%
Infection Protection:
- Treats Cuts, Scrapes, Blisters and Bites
- Gently Sanitizes Skin Without Overdrying
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INGREDIENTS AND APPEARANCE
TN DICKINSONS WITCH HAZEL ANTIBACTERIAL
benzethonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52651-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength benzethonium chloride (UNII: PH41D05744) (benzethonium - UNII:1VU15B70BP) benzethonium chloride 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength witch hazel (UNII: 101I4J0U34) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52651-006-01 1 in 1 CARTON 1 120 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/01/2012 Labeler - Dickinson Brands Inc. (124620340)