Label: HUMCO WITCH HAZEL- witch hazel liquid
- NDC Code(s): 0395-3213-16
- Packager: Humco Holding Group, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 15, 2023
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- When using this product stop use and consult a doctor if:
- Keep out of reach of children.
- Directions
- Inactive ingredents
- Label
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INGREDIENTS AND APPEARANCE
HUMCO WITCH HAZEL
witch hazel liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0395-3213 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) WITCH HAZEL 884 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0395-3213-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 02/01/2012 Labeler - Humco Holding Group, Inc. (825672884) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(0395-3213) , analysis(0395-3213) , pack(0395-3213) , label(0395-3213)