Label: ADVANCED HAND SANITIZER- alcohol gel
- NDC Code(s): 41250-439-16, 41250-439-34, 41250-439-45
- Packager: Meijer Distribution, Inc
- 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 March 2, 2022
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- 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
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SPL UNCLASSIFIED SECTION
Questions? Call 1-888-593-0593
**Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds
*This product is not manufactured or distributed by GOJO Industries, Inc distributor of Purell Refreshing Aloe Advanced Hand Sanitizer
Patent Pending Made in U.S. with U.S. and foreign parts
DISTRIBUTED BY
MEIJER DISTRIBUTION, INC
GRAND RAPIDS, MI 49544 - principal display panel
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INGREDIENTS AND APPEARANCE
ADVANCED HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-439 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 616 mL in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOMER COPOLYMER TYPE b (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) SULISOBENZONE (UNII: 1W6L629B4K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-439-16 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/13/2013 2 NDC:41250-439-34 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/13/2013 3 NDC:41250-439-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/13/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/13/2013 Labeler - Meijer Distribution, Inc (006959555) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(41250-439) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(41250-439)