Label: WITCH HAZEL spray
- NDC Code(s): 79481-0617-1
- Packager: Meijer Distribution Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 13, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
- Directions
- Other information
- Inactive ingredient
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INGREDIENTS AND APPEARANCE
WITCH HAZEL
witch hazel sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79481-0617 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 860 mg in 1 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79481-0617-1 170 g in 1 CAN; Type 0: Not a Combination Product 08/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 08/27/2023 Labeler - Meijer Distribution Inc (006959555)