Label: CVS THERAPEUTIC MENTHOL GEL- menthol gel
- NDC Code(s): 59779-118-08
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 15, 2024
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- Active Ingredient
- Purpose
- Uses
- Warnings
- Do not use
- Ask a doctor before use
- When using this product
- If pregnant or breast-feeding
- Keep out of reach of children
- Directions
- Other information
- Other ingredients
- Product Label
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INGREDIENTS AND APPEARANCE
CVS THERAPEUTIC MENTHOL GEL
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-118 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2 g in 100 g Inactive Ingredients Ingredient Name Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ISOPROPYL ALCOHOL (UNII: ND2M416302) SODIUM HYDROXIDE (UNII: 55X04QC32I) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) Product Characteristics Color blue Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-118-08 227 g in 1 JAR; Type 0: Not a Combination Product 10/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 10/01/2014 Labeler - CVS Pharmacy (062312574) Registrant - Unipack LLC (116015769) Establishment Name Address ID/FEI Business Operations Unipack LLC 009248480 manufacture(59779-118)