Label: VELATRIN PAIN RELIEF- methyl salicylate, menthol, unspecified form cream
- NDC Code(s): 70287-716-01
- Packager: Quality Nature, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients:
- Uses:
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Warnings:
For external use only. If you had prior allergic reaction to aspirin or salicylate, please consult a physician before use. Allergy Alert:
Do not use
• on wounds or damaged skin • with a heating pad. you have redness over the affected area. Ask a Physician before use if
- Directions:
- Other information:
-
Inactive Ingredients:
Acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis (aloe vera gel) juice, aqua (deionized water), arnica montana (arnica) extract, camellia sinensis (green tea) leaf extract, citrus aurantium dulcis (orange) peel oil, citrus medica limonum (lemon) extract, ethylhexylglycerin, helianthus annuus (sunflower) seed oil, isopropyl myristate, PEG-8, phenoxyethanol, pyridoxine (vitamin B6), sodium lauryl sulfate, triethanolamine.
- Package Labeling:
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INGREDIENTS AND APPEARANCE
VELATRIN PAIN RELIEF
methyl salicylate, menthol, unspecified form creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70287-716 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 mg in 1 g MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 10 mg in 1 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARNICA MONTANA (UNII: O80TY208ZW) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ORANGE OIL (UNII: AKN3KSD11B) LEMON (UNII: 24RS0A988O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SUNFLOWER OIL (UNII: 3W1JG795YI) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PHENOXYETHANOL (UNII: HIE492ZZ3T) PYRIDOXINE (UNII: KV2JZ1BI6Z) SODIUM LAURYL SULFATE (UNII: 368GB5141J) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70287-716-01 113 g in 1 JAR; Type 0: Not a Combination Product 02/09/2017 04/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/25/2015 04/01/2024 Labeler - Quality Nature, Inc. (080014569)