Label: CVS THERAPEUTIC MENTHOL GEL- menthol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-118-08 - Packager: CVS Pharmacy
- 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 December 15, 2021
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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 not final part348 10/01/2014 Labeler - CVS Pharmacy (062312574) Establishment Name Address ID/FEI Business Operations Unipack, Inc. 009248480 manufacture(59779-118)