Label: BENZOCAINE,ISOPROPYL ALCOHOL swab
-
Contains inactivated NDC Code(s)
NDC Code(s): 44224-3623-0 - Packager: Adventure Ready Brands
- 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 December 21, 2021
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)
- Drug Facts
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BENZOCAINE,ISOPROPYL ALCOHOL
benzocaine,isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-3623 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 60 mg in 1 mL ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.6 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44224-3623-0 0.4 mL in 1 POUCH; Type 0: Not a Combination Product 01/03/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 01/03/2022 Labeler - Adventure Ready Brands (064437304) Registrant - Adventure Ready Brands (064437304) Establishment Name Address ID/FEI Business Operations Adventure Ready Brands 064437304 manufacture(44224-3623)