Label: PURELL ADVANCED HAND SANITIZER MOISTURIZING 2IN1 FOAM- alcohol liquid
- NDC Code(s): 21749-851-10
- Packager: GOJO Industries, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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Inactive ingredients
Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Avena Sativa (Oat) Kernel Extract, Canarium Luzonicum Gum Nonvolatiles, Caprylyl glycol, Citrus Aurantifolia (Lime) Peel Oil, Citrus Aurantium Bergamia (Bergamot) Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Glycerin, Isopropyl Myristate, Litsea Cubeba Fruit Oil, Mentha Arvensis Leaf Oil, Mentha Viridis (Spearmint) Leaf Oil, Niaciniamide, Pinus Silvestrus Leaf Oil, Pogostemon Cablin Oil, PPG-12/SMDI copolymer, Schinus Molle Oil, Tocopheryl Acetate, Potassium Sorbate
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INGREDIENTS AND APPEARANCE
PURELL ADVANCED HAND SANITIZER MOISTURIZING 2IN1 FOAM
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21749-851 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95) OAT (UNII: Z6J799EAJK) ELEMI (UNII: C13XI009KO) CAPRYLYL GLYCOL (UNII: 00YIU5438U) LIME OIL (UNII: UZH29XGA8G) BERGAMOT OIL (UNII: 39W1PKE3JI) ORANGE OIL (UNII: AKN3KSD11B) LEMON OIL (UNII: I9GRO824LL) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) LITSEA OIL (UNII: 2XIW34BN6O) MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N) SPEARMINT OIL (UNII: C3M81465G5) NIACINAMIDE (UNII: 25X51I8RD4) PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y) PATCHOULI OIL (UNII: F3IN55X5PO) PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E) SCHINUS MOLLE FRUIT OIL (UNII: 99O5U5NLK2) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21749-851-10 295 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/15/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 04/15/2021 Labeler - GOJO Industries, Inc. (004162038) Establishment Name Address ID/FEI Business Operations GOJO Industries, Inc. 036424534 manufacture(21749-851) , pack(21749-851) , label(21749-851)