Label: LIDOZEN PATCH- lidocaine, menthol patch
- NDC Code(s): 71205-745-05, 71205-745-15, 71205-745-30
- Packager: Proficient Rx LP
- This is a repackaged label.
- Source NDC Code(s): 71574-905
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 1, 2023
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- Official Label (Printer Friendly)
- DRUG FACTS:
- ACTIVE INGREDIENTS:
- USES:
- WARNINGS:
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DIRECTIONS (Adults and Children Over 12 Years):
Clean and dry affected area.
Remove patch from backing and apply to affected area.
Use only one patch at a time, and maximum of four patches / day.
Leave patch on affected area for up to 8-hours.
Do not use patches for longer than five consecutive days.
Children under 12 should consult physician prior to use.
- INACTIVE INGREDIENTS
- SPL UNCLASSIFIED SECTION
- Package Labeling:
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INGREDIENTS AND APPEARANCE
LIDOZEN PATCH
lidocaine, menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71205-745(NDC:71574-905) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 g MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 10 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYSORBATE 80 (UNII: 6OZP39ZG8H) TARTARIC ACID (UNII: W4888I119H) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) METHYLPARABEN (UNII: A2I8C7HI9T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71205-745-05 5 in 1 BOX 01/18/2023 1 1 g in 1 PATCH; Type 0: Not a Combination Product 2 NDC:71205-745-15 15 in 1 BOX 01/18/2023 2 1 g in 1 PATCH; Type 0: Not a Combination Product 3 NDC:71205-745-30 30 in 1 BOX 01/18/2023 3 1 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 09/01/2022 Labeler - Proficient Rx LP (079196022) Establishment Name Address ID/FEI Business Operations Proficient Rx LP 079196022 RELABEL(71205-745)