Label: MUSCLE RUB ULTRA STRENGTH CVS- camphor 4.00% menthol 10.00% methyl salicylate 30.00% spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 59779-492-04 - Packager: CVS
- 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 1, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients Purpose
- PURPOSE
-
WarningFor external use only
Flammable.
• do not use while smoking or near heat or flame
• avoid long term storage above 104oF
• do not puncture or incinerate. Contents under pressure
• do not store at temperature above 120oFWhen using this product
• avoid contact with eyes and mucous membranes
• do not apply to wounds or damages skin
• do not bandage tightly or use with a heating pad
• use only as directed - Uses
- Directions
- Inactive Ingredient
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MUSCLE RUB ULTRA STRENGTH CVS
camphor 4.00% menthol 10.00% methyl salicylate 30.00% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-492 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 4 g in 100 g Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) Menthol 10 g in 100 g Methyl Salicylate (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) Methyl Salicylate 30 g in 100 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-492-04 113 g in 1 CAN; Type 0: Not a Combination Product 12/22/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 12/22/2014 Labeler - CVS (062312574) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(59779-492)