Label: WITCH HAZEL liquid
- NDC Code(s): 10733-801-08, 10733-801-16
- Packager: Medical Products Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- Warnings
- Witch Hazel For Face & Body
- 10733-801-08
- 10733-801-16
-
INGREDIENTS AND APPEARANCE
WITCH HAZEL
witch hazel liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10733-801 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 86 g in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10733-801-08 236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 01/29/2021 2 NDC:10733-801-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/29/2021 11/30/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 01/29/2021 Labeler - Medical Products Laboratories, Inc. (002290302)