Label: MENTHOL DAVIS ANALGESIC- menthol ointment
- NDC Code(s): 82480-000-01
- Packager: Genia Care Phamaceutical S.A.
- 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 June 13, 2022
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INGREDIENTS AND APPEARANCE
MENTHOL DAVIS ANALGESIC
menthol ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82480-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 50 mg in 1 g Inactive Ingredients Ingredient Name Strength PARAFFIN (UNII: I9O0E3H2ZE) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82480-000-01 1 in 1 BLISTER PACK 09/04/2023 1 28 g in 1 CAN; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 09/04/2023 Labeler - Genia Care Phamaceutical S.A. (817305769)