Label: AFTER BITE WIPE- ethyl alcohol, lidocaine hcl liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 44224-3621-0 - Packager: Tender Corporation
- 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 November 4, 2016
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Do Not Use
- Stop use and ask a doctor
- Keep out of reach of children
- Directions
- Inactive Ingredients
- After Bite
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INGREDIENTS AND APPEARANCE
AFTER BITE WIPE
ethyl alcohol, lidocaine hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-3621 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL in 1 mL Inactive Ingredients Ingredient Name Strength MENTHOL (UNII: L7T10EIP3A) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44224-3621-0 1.1 mL in 1 POUCH; Type 0: Not a Combination Product 11/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/01/2016 Labeler - Tender Corporation (064437304) Registrant - Tender Corporation (064437304) Establishment Name Address ID/FEI Business Operations Tender Corporation 064437304 manufacture(44224-3621)