Label: WITCH HAZEL liquid
- NDC Code(s): 42681-7353-1
- Packager: Whole Foods Market
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 November 10, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredient
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Principal Display Panel
astringent
WITCH HAZEL
14% alcohol by volume
For Face and Body
Compare to T.N. Dickinson's® Witch Hazel*
Questions or comments?
customer, questions@wholefoods.com 1-844-936-8255
FL OZ (mL)
*This product is not manufactured or distributed by Dickinson Brands, Inc., distributor of T.N. Dickinson's® Witch Hazel
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
DISTRIBUTED BY: WHOLE FOODS MARKET
550 BOWIE STREET, AUSTIN, TX 78703
- Package Label
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INGREDIENTS AND APPEARANCE
WITCH HAZEL
witch hazel liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42681-7353 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 842 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42681-7353-1 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/31/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 03/31/2018 Labeler - Whole Foods Market (196175616)