ETHYL ALCOHOL- ethyl alcohol liquid 
Chemco Corporation

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.

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49283-050-70

wipes

ETHYL ALCOHOL 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49283-050
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 2 mL  in 100 mL
WATER (UNII: 059QF0KO0R) 37.9 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.1 mL  in 100 mL
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49283-050-7050 mL in 1 PACKAGE; Type 0: Not a Combination Product06/05/2020
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/05/2020
Labeler - Chemco Corporation (032495954)
Registrant - Chemco Corporation (032495954)
Establishment
NameAddressID/FEIBusiness Operations
Chemco Corporation032495954manufacture(49283-050)

Revised: 6/2020
Document Id: a7593e39-a3a5-159f-e053-2995a90aee6d
Set id: a5c6d6be-5b17-a625-e053-2995a90af5a9
Version: 2
Effective Time: 20200605
 
Chemco Corporation