Label: MINT RX ENDURANCE WIPES- benzocaine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 77691-433-03, 77691-433-08 - Packager: PHARMAMEDRX
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 20, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Keep out of reach of children
- Use
- Warnings
- Stop use and ask a doctor if
- Directions
- Inactive ingredients
- MINT RX ENDURANCE WIPESBENZOCAINE USP 5%
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INGREDIENTS AND APPEARANCE
MINT RX ENDURANCE WIPES
benzocaine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77691-433 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77691-433-08 8 in 1 PACKAGE 05/20/2020 1 NDC:77691-433-03 2 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 05/20/2020 Labeler - PHARMAMEDRX (063814205) Registrant - PHARMAMEDRX (063814205) Establishment Name Address ID/FEI Business Operations PHARMAMEDRX 063814205 manufacture(77691-433)