NDC | 21749-625-01, 21749-625-02, 21749-625-08, 21749-625-10, 21749-625-12, 21749-625-28, 21749-625-29 |
Set ID | b36013d2-96a6-4c40-ad05-8d9c0d9cdb1f |
Category | HUMAN OTC DRUG LABEL |
Packager | GOJO Industries, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
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Inactive Ingredients:
Water (Aqua), Isopropyl Alcohol, Caprylyl glycol, Citrus Aurantium Dulcis (Orange) Peel Oil, Glycerin, Isopropyl Myristate, Lavandula Hybrida (Lavandin) oil, Litsea Cubeba Fruit Oil, Pelargonium Graevolens (Geranium) oil, Pogostemon Cablin Oil, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PURELL ADVANCED HAND SANITIZER NATURALS GEL
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-625 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) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) BITTER ORANGE OIL (UNII: 9TLV70SV6I) LAVANDIN OIL (UNII: 9RES347CKG) LITSEA OIL (UNII: 2XIW34BN6O) GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PATCHOULI OIL (UNII: F3IN55X5PO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-625-01 30 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 2 NDC:21749-625-02 59 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 3 NDC:21749-625-04 118 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/15/2019 4 NDC:21749-625-08 236 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 5 NDC:21749-625-29 295 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 6 NDC:21749-625-12 355 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 7 NDC:21749-625-28 828 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 8 NDC:21749-625-10 1000 mL in 1 PACKAGE; Type 0: Not a Combination Product 01/01/2016 9 NDC:21749-625-24 710 mL in 1 PACKAGE; Type 0: Not a Combination Product 08/01/2021 10 NDC:21749-625-65 192 mL in 1 PACKAGE; Type 0: Not a Combination Product 07/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/01/2016 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-625) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 088312414 manufacture(21749-625) , label(21749-625) , pack(21749-625)