Label: PREFERRED PLUS ARTHRITIS CREAM- menthol topical analgesic cream
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Contains inactivated NDC Code(s)
NDC Code(s): 61715-032-02 - Packager: Kinray
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated March 1, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warning
- Ask Doctor
- If pregnant or breast feeding
- Keep out of reach of children
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Directions
- apply to the affective area and gently rub it in until fully absorbed
- repeat asnecessary, but not more than 3 to 4 times daily.
- for best results use continuously for 2 to 4 weeks
- avoid washing treated area for at least 30 minutes after application
- unless treating hands, wash hands thoroughly with soap and water immediately after use
Children under 12
consult a doctor - Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PREFERRED PLUS ARTHRITIS CREAM
menthol topical analgesic creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61715-032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 15 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 g in 100 g CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.025 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) PEG-40 STEARATE (UNII: ECU18C66Q7) STEARETH-2 (UNII: V56DFE46J5) TROLAMINE (UNII: 9O3K93S3TK) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) CARBOMER 940 (UNII: 4Q93RCW27E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61715-032-02 58 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/23/2001 Labeler - Kinray (012574513) Registrant - Reese Pharmaceutical Co (004172052) Establishment Name Address ID/FEI Business Operations Reese Pharmaceutical Co 004172052 relabel(61715-032) , repack(61715-032)