Label: PURELL ADVANCED INSTANT HAND SANITIZER- alcohol liquid
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NDC Code(s):
21749-700-00,
21749-700-01,
21749-700-02,
21749-700-03, view more21749-700-04, 21749-700-07, 21749-700-08, 21749-700-10, 21749-700-12, 21749-700-15, 21749-700-20, 21749-700-29, 21749-700-45, 21749-700-47, 21749-700-59, 21749-700-60, 21749-700-67, 21749-700-80, 21749-700-89
- Packager: GOJO Industries, Inc.
- 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 February 24, 2022
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- Active ingredient
- Purpose
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- Warnings
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- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURELL ADVANCED INSTANT HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-700 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.70 mL in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Isopropyl Alcohol (UNII: ND2M416302) Glycerin (UNII: PDC6A3C0OX) Isopropyl Myristate (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) Caprylyl Glycol (UNII: 00YIU5438U) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-700-02 24 in 1 CASE 05/10/2011 1 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:21749-700-10 8 in 1 CASE 05/10/2011 2 1000 mL in 1 BAG; Type 0: Not a Combination Product 3 NDC:21749-700-89 4 in 1 CASE 05/10/2011 3 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:21749-700-20 4 in 1 CASE 05/10/2011 4 2000 mL in 1 BAG; Type 0: Not a Combination Product 5 NDC:21749-700-67 4 in 1 CASE 05/10/2011 5 2000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 6 NDC:21749-700-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 7 NDC:21749-700-80 800 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 8 NDC:21749-700-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 9 NDC:21749-700-07 222 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 10 NDC:21749-700-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 11 NDC:21749-700-59 590 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 12 NDC:21749-700-15 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 13 NDC:21749-700-60 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 14 NDC:21749-700-47 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 15 NDC:21749-700-03 89 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 16 NDC:21749-700-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/10/2011 17 NDC:21749-700-00 1.2 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2016 18 NDC:21749-700-45 450 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 19 NDC:21749-700-29 295 mL in 1 PACKAGE; Type 0: Not a Combination Product 09/28/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/10/2011 Labeler - GOJO Industries, Inc. (004162038) Registrant - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-700) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 manufacture(21749-700) , label(21749-700) , pack(21749-700) Establishment Name Address ID/FEI Business Operations Travis Association for the Blind 026032268 pack(21749-700)