Label: PURE SOURCE HAND SANITIZER- alcohol gel
- NDC Code(s): 65121-054-02, 65121-054-16
- Packager: Pure Source, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- USES
- Warnings
- Directions:
- Other information:
- Inactive ingredients
- QUESTIONS
- Package Labeling: 65121-054-02
- Package Labeling: 65121-054-16
-
INGREDIENTS AND APPEARANCE
PURE SOURCE HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65121-054 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 CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) ALOE VERA LEAF (UNII: ZY81Z83H0X) AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ) WATER (UNII: 059QF0KO0R) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 20 (UNII: 7T1F30V5YH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65121-054-02 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2020 01/01/2023 2 NDC:65121-054-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/10/2020 01/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 04/01/2020 01/01/2023 Labeler - Pure Source, LLC (080354456)