Label: GENRX ANTI-BACTERIAL GEL- alcohol liquid
- NDC Code(s): 59088-299-08, 59088-299-31, 59088-299-39, 59088-299-48
- Packager: PureTek Corporation
- Category: HUMAN OTC DRUG LABEL
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 August 18, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- GenRx Hand Sanitizing Gel (24 fl oz)
-
INGREDIENTS AND APPEARANCE
GENRX ANTI-BACTERIAL GEL
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-299 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength SHEA BUTTER (UNII: K49155WL9Y) AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) PANTHENOL (UNII: WV9CM0O67Z) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-299-48 710 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/18/2020 05/11/2020 2 NDC:59088-299-08 118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/18/2020 3 NDC:59088-299-31 500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 03/18/2020 4 NDC:59088-299-39 710 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/18/2020 Labeler - PureTek Corporation (785961046) Establishment Name Address ID/FEI Business Operations PureTek Corporation 785961046 manufacture(59088-299)