Label: KELLYS DELIGHT HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 79175-002-01, 79175-002-02, 79175-002-03, 79175-002-04, view more79175-002-05, 79175-002-06, 79175-002-07, 79175-002-08, 79175-002-09, 79175-002-10, 79175-002-11 - Packager: WACO BOTTLING LLC
- 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 November 14, 2022
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- Active Ingredient
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- Inactive ingredients
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INGREDIENTS AND APPEARANCE
KELLYS DELIGHT HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79175-002 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 GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) ADENOSINE PHOSPHATE (UNII: 415SHH325A) ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DIPROPYLENE GLYCOL (UNII: E107L85C40) LEMON OIL (UNII: I9GRO824LL) LINALYL ACETATE (UNII: 5K47SSQ51G) LINALOOL, (+/-)- (UNII: D81QY6I88E) GERANIOL (UNII: L837108USY) TERPINEOL (UNII: R53Q4ZWC99) CITRAL (UNII: T7EU0O9VPP) 4-TERT-BUTYLCYCLOHEXYL ACETATE (UNII: 21EUM2B8UC) .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79175-002-01 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 2 NDC:79175-002-02 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 3 NDC:79175-002-03 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 4 NDC:79175-002-04 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 5 NDC:79175-002-05 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 6 NDC:79175-002-06 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 7 NDC:79175-002-07 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 8 NDC:79175-002-08 1893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 9 NDC:79175-002-09 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 10 NDC:79175-002-10 18927 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 11 NDC:79175-002-11 208198 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/08/2020 Labeler - WACO BOTTLING LLC (080331158) Establishment Name Address ID/FEI Business Operations WACO BOTTLING LLC 080331158 manufacture(79175-002)