Label: TURMERIC PAIN RELIEVING CREAM- methyl salicylate, menthol, camphor cream cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72982-1903-1 - Packager: Everyday Medical LLC
- 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 January 13, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only
When using this product: Use only as directed
- do not bandage tightly or use with a heating pad
- avoid contact with eyes and mucous membranes
- do not apply to wounds or damaged, broken or irritated skin
- if severe burning sensation occurs, discontinue use immediately
Stop use and ask a doctor if
- condition worsens
- redness is present
- irritation develops
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TURMERIC PAIN RELIEVING CREAM
methyl salicylate, menthol, camphor cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72982-1903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5 g in 100 g CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 4 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength LINSEED OIL (UNII: 84XB4DV00W) WATER (UNII: 059QF0KO0R) ARNICA MONTANA (UNII: O80TY208ZW) BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ) CURCUMIN (UNII: IT942ZTH98) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARIC ACID (UNII: 4ELV7Z65AP) COMFREY (UNII: D05HXK6R3G) EMU OIL (UNII: 344821WD61) CETETH-20 (UNII: I835H2IHHX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72982-1903-1 141 g in 1 CONTAINER; Type 0: Not a Combination Product 04/08/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/08/2019 Labeler - Everyday Medical LLC (117001767) Registrant - Everyday Medical LLC (117001767)