Label: KAY ACTIGEL- ethanol solution
- NDC Code(s): 63146-301-02
- Packager: Kay Chemical Company
- 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 July 14, 2023
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Principal Display Panel/Representative Label
NDC NO.: 63146-301-02
Kay
Actigel
Hand Sanitizer
To obtain instruction in Spanish, see outer carton.
ECOLAB
KAY CHEMICAL COMPANY
8300 Capital Drive
Greensboro, NC 27409-9790, USA
Customer Service: (800) 529-5458
SDS-NC-872
27 US fl oz (800 ml)
722473-03
FRSUSA 722473/8003/0910
©2010 Kay Chemical Company
All Rights Reserved
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INGREDIENTS AND APPEARANCE
KAY ACTIGEL
ethanol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 60 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) TROLAMINE (UNII: 9O3K93S3TK) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MYRISTYL ALCOHOL (UNII: V42034O9PU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63146-301-02 800 mL in 1 BAG; Type 0: Not a Combination Product 05/26/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/26/2010 Labeler - Kay Chemical Company (003237021)