![PURELL ADVANCED FOAM HAND RUB (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]](https://medic.hrt.org//dailymed/images/f67dac52-88d9-4d46-84db-517b01acdcd9/d4079d60-d213-4508-b5f1-4961de7fe696.jpg)
| NDC | 21749-982-45, 21749-982-53, 21749-982-89, 21749-982-97 |
| Set ID | f67dac52-88d9-4d46-84db-517b01acdcd9 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | GOJO Industries, Inc. |
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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 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)
