Label: TE-FU RECOVERY MASSAGE- menthol, methyl salicylate lotion
- NDC Code(s): 44717-539-01
- Packager: Wasatch Product Development
- 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 November 30, 2022
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients: Water, Cinnamomium Camphora (Camphor) Bark Oil, Stearyl Alcohol, C13-15 Alkane, Glycerin, Caprylic/capric Triglyceride, Pentylene Glycol, Glyceryl Stearate, Cetearyl Alcohol, Eucalyptus Globulus Leaf Oil, Prunus Amygdalus Dulcis( sweet almond) Oil, Microcrystalline Cellulose, Mentha Piperita (peppermint) Oil, Behenyl Alcohol, Stearyl Phosphate, Eugenia Caryophyllus (Clove) Leaf Oil, Hydroxyacetophenone, Zingiber Officinale (ginger) Root Oil, Arnica Montana Flower Extract, Benzyl Alcohol, Cellulose Gum, Cyamopsis Tetragonoloba (Guar) Gum, Xanthan Gum, Sodium Phytate.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TE-FU RECOVERY MASSAGE
menthol, methyl salicylate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44717-539 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5 g in 100 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 10 g in 100 mL Inactive Ingredients Ingredient Name Strength CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) EUCALYPTUS OIL (UNII: 2R04ONI662) STEARYL PHOSPHATE (UNII: F3C8G3904Y) PEPPERMINT OIL (UNII: AV092KU4JH) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) GUAR GUM (UNII: E89I1637KE) XANTHAN GUM (UNII: TTV12P4NEE) CAMPHOR OIL (UNII: 75IZZ8Y727) CLOVE LEAF OIL (UNII: VCA5491KVF) BENZYL ALCOHOL (UNII: LKG8494WBH) PHYTATE SODIUM (UNII: 88496G1ERL) C13-15 ALKANE (UNII: 114P5I43UJ) GLYCERIN (UNII: PDC6A3C0OX) ALMOND OIL (UNII: 66YXD4DKO9) GINGER OIL (UNII: SAS9Z1SVUK) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) PENTYLENE GLYCOL (UNII: 50C1307PZG) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) WATER (UNII: 059QF0KO0R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) DOCOSANOL (UNII: 9G1OE216XY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44717-539-01 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/28/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/28/2018 Labeler - Wasatch Product Development (962452533)