Label: CVS THERAPEUTIC MENTHOL PAIN RELIEVER- menthol gel
- Category: HUMAN OTC DRUG LABEL
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.
Updated July 10, 2010
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- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
For external use only
When using this product
- do not bandage tightly - avoid contact with the eyes
- do not apply to wounds or damaged skin
- do not use with heating pads or other heating devices
Stop use and ask a doctor if - condition worsens or if symptoms persist
for more than 7 days or clear up and occur again within a few days
Keep out of reach of children.If swallowed, get medical help or contact a
Poison Control Center right away.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
CVS THERAPEUTIC MENTHOL PAIN RELIEVER
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-056 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 20 mg in 1 g Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) CARBOMER 934 (UNII: Z135WT9208) WATER (UNII: 059QF0KO0R) THYMOL (UNII: 3J50XA376E) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-056-36 1 in 1 CARTON 1 227 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part348 07/10/2010 Labeler - CVS Pharmacy (062312574) Registrant - Pharma Pac, LLC (140807475) Establishment Name Address ID/FEI Business Operations Pharma Pac, LLC 140807475 manufacture