Label: FELIX HAND SANITIZER GEL- alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 74004-702-01 - Packager: Ester Co., Ltd.
- 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 May 21, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
FELIX HAND SANITIZER GEL
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74004-702 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 350 mL in 500 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) GREEN TEA LEAF (UNII: W2ZU1RY8B0) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) EDETOL (UNII: Q4R969U9FR) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74004-702-01 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/21/2020 Labeler - Ester Co., Ltd. (688425766) Establishment Name Address ID/FEI Business Operations Ester Co., Ltd. 688425766 manufacture(74004-702)