Label: CAPASIL PAIN RELIEVING- menthol, methyl salicylate cream
- NDC Code(s): 59088-434-05
- Packager: PureTek Corporation
- 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 October 14, 2020
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Keep out of reach of children.
- Uses
- Warnings
- Directions
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Inactive ingredients
Aloe Barbadensis(Aloe Vera) Leaf Juice Powder, Aqua (Purified Water), Borago Officinalis Seed
Oil, Carbomer, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, DL-alpha-tocopheryl
acetate, Eucalyptus Globulus Leaf Oil, Fragrance, Fructose, Phenoxyethanol,
Propylene Glycol, Squalane, Stearic Acid, Stearyl Alcohol, Sodium Hydroxide,
Tetrasodium EDTA, Vitis Vinifera (Grape) Seed Oil. - STORAGE AND HANDLING
- Label
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INGREDIENTS AND APPEARANCE
CAPASIL PAIN RELIEVING
menthol, methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-434 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 100 mg in 1 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength MENHADEN OIL (UNII: 1D8HWC57D0) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ) LIMONENE, (+)- (UNII: GFD7C86Q1W) PALMITIC ACID (UNII: 2V16EO95H1) ALOE VERA LEAF (UNII: ZY81Z83H0X) BORAGE SEED OIL (UNII: F8XAG1755S) CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) EUCALYPTUS OIL (UNII: 2R04ONI662) FRUCTOSE (UNII: 6YSS42VSEV) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) SQUALANE (UNII: GW89575KF9) STEARIC ACID (UNII: 4ELV7Z65AP) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) GRAPE SEED OIL (UNII: 930MLC8XGG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-434-05 59 mL in 1 JAR; Type 0: Not a Combination Product 10/14/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/14/2020 Labeler - PureTek Corporation (785961046)