Label: STUDIO 35 EXTERNAL ANALGESIC MEDICATED BODY- menthol and zinc oxide powder
- NDC Code(s): 0363-0552-38
- Packager: Walgreen Co
- 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 February 8, 2017
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- Active Ingredients
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- Stop use and ask a doctor
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INGREDIENTS AND APPEARANCE
STUDIO 35 EXTERNAL ANALGESIC MEDICATED BODY
menthol and zinc oxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0552 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.5 mg in 1 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 10 mg in 1 g Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) SODIUM BICARBONATE (UNII: 8MDF5V39QO) TRICALCIUM PHOSPHATE (UNII: K4C08XP666) GUM TALHA (UNII: H18F76G097) EUCALYPTOL (UNII: RV6J6604TK) METHYL SALICYLATE (UNII: LAV5U5022Y) SALICYLIC ACID (UNII: O414PZ4LPZ) THYMOL (UNII: 3J50XA376E) ZINC STEARATE (UNII: H92E6QA4FV) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0552-38 283 g in 1 BOTTLE; Type 0: Not a Combination Product 02/07/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 02/07/2017 Labeler - Walgreen Co (008965063) Registrant - Jell Pharmaceuticals Pvt. Ltd. (726025211) Establishment Name Address ID/FEI Business Operations Jell Pharmaceuticals Pvt. Ltd. 726025211 manufacture(0363-0552)