Label: DR HO S PAIN RELIEF EXTRA STGHT- methyl salicylate,menthol,eucalyptus oil cream
- NDC Code(s): 71447-187-00, 71447-187-01
- Packager: LABORATOIRES DRUIDE INC
- 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, 2023
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- Official Label (Printer Friendly)
- DRUG FACTS
- ACTIVE INGREDIENTS
- Purpose
- USES
- WARNINGS
- When using this product
- Stop use and ask a doctor
- Keep safely out of reach of children
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DIRECTIONS
■ For use on adults and children over 12 years of age.
■ Apply generously to the affected area using hands-free applicator ■ Use 3 to 4 times per day as required. A stinging or burning sensation will be experienced during the first few minutes as the formula begins working. For arthritis or muscle pain of the hands, retain for at least 10 minutes then wash hands.
- INACTIVE INGREDIENTS
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- DR-HO'S PAIN RELIEF STICK EXTRA STRENGHT 1.86 OZ (53G) (NDC 71447-187-00)
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INGREDIENTS AND APPEARANCE
DR HO S PAIN RELIEF EXTRA STGHT
methyl salicylate,menthol,eucalyptus oil creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71447-187 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 30 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 15 g in 100 g EUCALYPTUS OIL (UNII: 2R04ONI662) (EUCALYPTUS OIL - UNII:2R04ONI662) EUCALYPTUS OIL 1 g in 100 g Inactive Ingredients Ingredient Name Strength COCOS NUCIFERA WHOLE (UNII: 245J88W96L) BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU) TOCOPHEROL (UNII: R0ZB2556P8) PARAFFIN (UNII: I9O0E3H2ZE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71447-187-01 1 in 1 BOX 02/08/2023 1 NDC:71447-187-00 53 g in 1 TUBE, WITH APPLICATOR; 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 02/08/2023 Labeler - LABORATOIRES DRUIDE INC (245815014) Registrant - LABORATOIRES DRUIDE INC (245815014) Establishment Name Address ID/FEI Business Operations LABORATOIRES DRUIDE INC 245815014 manufacture(71447-187)