Label: QSR HAND SANITIZER- alcohol solution
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NDC Code(s):
63146-112-02,
63146-112-07,
63146-112-08,
63146-112-09, view more63146-112-14
- Packager: Kay Chemical Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 26, 2024
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Principal display panel and representative label
NDC 63146-112-09 KAY
QSR
Hand Sanitizer
FOR INSTITUTIONAL USE ONLY
Ethanol 60% by volume
Net contents: 40.6 US fl oz (1200 mL)
Meets the requirements for Hand Antiseptics as specified in section 2-301.16 of the 2017 Food Code.
(2017 Food Code).
SDS-NC-872, SDS-NJ-20007
Distributed by
Kay Chemical Company
8300 Capital Drive · Greensboro, NC 27409-9790 USA Customer Service: (800) 529-5458
©2020 Kay Chemical Company
All rights reserved | KUSA 756614/8004/1020
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INGREDIENTS AND APPEARANCE
QSR HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 534 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) TROLAMINE (UNII: 9O3K93S3TK) CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MYRISTYL ALCOHOL (UNII: V42034O9PU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63146-112-02 800 mL in 1 BAG; Type 0: Not a Combination Product 02/23/2010 2 NDC:63146-112-07 37 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/23/2010 05/02/2024 3 NDC:63146-112-08 750 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/23/2010 11/30/2022 4 NDC:63146-112-09 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/23/2010 5 NDC:63146-112-14 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 02/23/2010 Labeler - Kay Chemical Company (003237021)