Label: FOAMING SANITIZING HAND- alcohol soap
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NDC Code(s):
50865-710-17,
50865-710-41,
50865-710-44,
50865-710-55, view more50865-710-91
- Packager: Kutol Products Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
FOAMING SANITIZING HAND
alcohol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50865-710 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.072 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50865-710-41 1000 mL in 1 BAG; Type 0: Not a Combination Product 12/01/2015 2 NDC:50865-710-17 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2015 3 NDC:50865-710-44 1000 mL in 1 BAG; Type 0: Not a Combination Product 10/01/2015 4 NDC:50865-710-55 1200 mL in 1 BAG; Type 0: Not a Combination Product 10/01/2015 5 NDC:50865-710-91 532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/01/2015 Labeler - Kutol Products Company (004236139) Registrant - Kutol Products Company (004236139) Establishment Name Address ID/FEI Business Operations Kutol Products Company 004236139 manufacture(50865-710)