Label: WINTER APPLE- hand sanitizer gel
- NDC Code(s): 30142-803-16
- Packager: Kroger, CO.,
- Category: HUMAN OTC DRUG LABEL
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 December 12, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- Principal Panel Display
-
INGREDIENTS AND APPEARANCE
WINTER APPLE
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-803 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) FD&C RED NO. 40 (UNII: WZB9127XOA) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-803-16 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/24/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/24/2016 Labeler - Kroger, CO., (006999528) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(30142-803) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(30142-803)