Label: DR. DS SUPER 7 PAIN RELIEF- menthyl salicylate and menthol cream
- NDC Code(s): 72246-112-01
- Packager: Promedx Innovations 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 January 27, 2021
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
Allergy alert
- do not use if you are allergic to plants of the Asteraceae / Compositae / Daisy family
When using this product
- avoid contact with the eyes and mucous membranes
- do not apply to wounds or damaged skin
- do not bandage tightly
- do not apply with external heat, such as an electric pad, as this may result in excessive skin irritation or skin burn
- Directions
- Other information
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Inactive ingredients
Arnica Montana Flower Extract, Benzoic Acid, Brassica Campestris (Rapeseed) Seed Oil, Citric Acid, Dehydroacetic Acid, Eucalyptus Globulus Leaf Essential Oil, Glycerin, Linum Usitatissimum (Linseed) Seed Extract, MSM, Myristyl Myristate, Neopentyl Glycol Dicaprylate/Dicaprate, Peppermint Oil (Mentha piperita), Phenoxyethanol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Silica, Sodium Stearoyl Glutamate, Water, Xanthan Gum
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INGREDIENTS AND APPEARANCE
DR. DS SUPER 7 PAIN RELIEF
menthyl salicylate and menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72246-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 20 mg in 1 mL MENTHYL SALICYLATE, (+/-)- (UNII: 43XOA705ZD) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) DEHYDROACETIC ACID (UNII: 2KAG279R6R) EUCALYPTUS OIL (UNII: 2R04ONI662) PEPPERMINT OIL (UNII: AV092KU4JH) NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) BRASSICA RAPA SUBSP. OLEIFERA OIL (UNII: N4G8379626) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ROSEMARY (UNII: IJ67X351P9) XANTHAN GUM (UNII: TTV12P4NEE) GLYCERIN (UNII: PDC6A3C0OX) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) FLAX SEED (UNII: 4110YT348C) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72246-112-01 1 in 1 CARTON 09/04/2019 1 88 mL in 1 BOTTLE, 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 09/04/2019 Labeler - Promedx Innovations Inc (203749853)