Label: SOFT CARE FOAM INSTANT HAND SANITIZER- alcohol liquid
- NDC Code(s): 64536-7295-4, 64536-7295-5
- Packager: Diversey, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Do not ingest
Do not use in the eyes.
When using this product do not get into the eyes.
In case of contact, immediately flush with water.
- DOSAGE & ADMINISTRATION
- REFERENCES
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SOFT CARE FOAM INSTANT HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64536-7295 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) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS) EDETATE DISODIUM (UNII: 7FLD91C86K) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64536-7295-5 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/03/2016 10/31/2022 2 NDC:64536-7295-4 532 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/03/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 08/03/2016 Labeler - Diversey, Inc. (018240817) Establishment Name Address ID/FEI Business Operations Kutol Products Company, Inc. 004236139 manufacture(64536-7295)