Label: CVS ARTHRITIS PAIN RELIEF- arthritis pain relief cream
- NDC Code(s): 69842-301-60
- Packager: CVS Health
- 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 August 31, 2016
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
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Inactive Ingredients
Deoinized Water, Emu Oil, Butylene Glycol, Polyacrylamide, Sodium Polyacrylate, C13-C14 Isoparaffin, Laureth-7, Methylsulfonylmethane, Hellanthus Annuus( Sunflower )Oil, Ethylhexyl Stearate, Glucosamine HCL, Chondroitin Sulfate, Tocopheryl Acetate, Trideceth-6, Tetrasodium EDTA, Potassium Sorbate, Methylisothiazolinone
- CVS Arthritis Cream 4 oz-jar
- CVS Arthritis Cream 4 oz -Carton
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INGREDIENTS AND APPEARANCE
CVS ARTHRITIS PAIN RELIEF
arthritis pain relief creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE .025 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) EMU OIL (UNII: 344821WD61) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIDECETH-6 (UNII: 3T5PCR2H0C) EDETATE SODIUM (UNII: MP1J8420LU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-301-60 1 in 1 CARTON 05/30/2016 1 113 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/30/2016 Labeler - CVS Health (062312574) Establishment Name Address ID/FEI Business Operations Sheffield Pharmaceuticals LLC 151177797 manufacture(69842-301)