Label: ALCOHOL SANITIZER- foaming alcohol sanitizer solution
- NDC Code(s): 73782-688-10, 73782-688-14, 73782-688-24
- Packager: Chemco Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 January 10, 2023
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INGREDIENTS AND APPEARANCE
ALCOHOL SANITIZER
foaming alcohol sanitizer solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73782-688 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) GLYCERIN (UNII: PDC6A3C0OX) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73782-688-10 1000 mL in 1 BAG; Type 0: Not a Combination Product 03/16/2020 2 NDC:73782-688-14 950 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/16/2020 3 NDC:73782-688-24 1000 mL in 1 BAG; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/16/2020 Labeler - Chemco Corporation (058342759) Registrant - Kutol Products Company (004236139) Establishment Name Address ID/FEI Business Operations Kutol Products Company 004236139 manufacture(73782-688)