Label: WITCH HAZEL liquid
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- NDC Code(s): 0869-0822-43
- Packager: Vi-Jon
- 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 September 13, 2022
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- Inactive ingredient
- SPL UNCLASSIFIED SECTION
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SWAN WITCH HAZEL USP
Hamamelis Water
- Skin Astringent
- For Relief of Minor Skin irritations Due to: Insect -Insect Bites - Minor Cuts -Minor Scrapes
Square bottle uses less plastic than a similarly sized round bottle. Recycle (if available in your area)
Compare to T.N. Dickinson's Witch Hazel*
16 FL OZ (1 PT) 473 mL
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INGREDIENTS AND APPEARANCE
WITCH HAZEL
witch hazel liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0822 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 kg in 100 L Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0869-0822-43 473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/29/1998 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 01/29/1998 Labeler - Vi-Jon (790752542) Registrant - Vi-Jon (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon 790752542 manufacture(0869-0822) Establishment Name Address ID/FEI Business Operations Vi-Jon 088520668 manufacture(0869-0822)
