Label: ADVANCED HAND SANITIZER- alcohol gel
- NDC Code(s): 63940-439-16, 63940-439-34, 63940-439-45
- Packager: Harmon Stores, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 22, 2024
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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
*This product is not manufactured or distributed by GOJO Industries, Inc. distributor of Purell Refreshing Aloe Advanced Hand Sanitizer
**Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds
Distributed by Harmon Stores, Inc
650 Liberty Ave., Union, NJ 07083 UA
Harmon Stores, Inc
Visit us at: www.facevalues.com - 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:63940-439 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 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:63940-439-34 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/18/2014 2 NDC:63940-439-16 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/18/2014 3 NDC:63940-439-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/18/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 02/18/2014 Labeler - Harmon Stores, Inc (804085293) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(63940-439) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(63940-439)