Label: MENTHOL PATCH patch
- NDC Code(s): 83675-010-01
- Packager: Guangzhou Hanhai Trading Co., Ltd
- 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 September 20, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Use
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MENTHOL PATCH
menthol patch patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83675-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 19 g in 100 Inactive Ingredients Ingredient Name Strength POWDERED CELLULOSE (UNII: SMD1X3XO9M) IVERMECTIN (UNII: 8883YP2R6D) DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (40/60 W/W; 1000000 PA.S) (UNII: 83D19O7250) BACKHOUSIA MYRTIFOLIA WHOLE (UNII: M5B93S0VJK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83675-010-01 8 in 1 BAG; Type 0: Not a Combination Product 09/19/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 09/19/2023 Labeler - Guangzhou Hanhai Trading Co., Ltd (419707381) Establishment Name Address ID/FEI Business Operations Guangzhou Hanhai Trading Co., Ltd 419707381 label(83675-010) , manufacture(83675-010)