Label: PURELL ADVANCED FOAM HAND RUB- alcohol liquid
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NDC Code(s):
21749-982-17,
21749-982-45,
21749-982-53,
21749-982-89, view more21749-982-97
- Packager: GOJO Industries, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated March 2, 2023
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURELL ADVANCED FOAM HAND RUB
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-982 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Isopropyl Alcohol (UNII: ND2M416302) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-982-45 45 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/15/2013 2 NDC:21749-982-53 535 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/15/2013 3 NDC:21749-982-97 700 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/15/2013 4 NDC:21749-982-89 1200 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/15/2013 5 NDC:21749-982-17 515 mL in 1 PACKAGE; Type 0: Not a Combination Product 08/08/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 01/15/2013 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-982)
