Label: WITCH HAZEL liquid
- NDC Code(s): 41190-822-43
- Packager: Wakefern Food Corp
- 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 12, 2022
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SPL UNCLASSIFIED SECTION
Sealed with printed foil under cap for your protection
Distributed by Wakefern Food Corporation
5000 Riverside Drive, Keasbey, NJ 08832
We welcome your questions or comments Call: 1-800-ShopRite (8 am-8 pm EST)
E-mail: www.shoprite.com
Write: Wakefern Food Corp.
Consumer Affairs P7-103
600 York St., Elizabeth, NJ 07027
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INGREDIENTS AND APPEARANCE
WITCH HAZEL
witch hazel liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41190-822 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:41190-822-43 .473 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1989 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 07/15/1989 Labeler - Wakefern Food Corp (069722418) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(41190-822) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(41190-822)