Label: EASE YOUR PAIN- menthol cream
- NDC Code(s): 72683-002-01
- Packager: Proximity Capital Partners LLC dba Asutra
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Use only as directed.
For external use only.Keep away from excessive heat or flame.
When using this product:
- Avoid contact with eyes and mucous membranes
- Do not apply to wounds or damaged skin
- Do not bandage or use with a heating pad, other ointments, creams, sprays, or liniments
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EASE YOUR PAIN
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72683-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 4 g in 100 g Inactive Ingredients Ingredient Name Strength ADANSONIA DIGITATA SEED OIL (UNII: 77MKL7AR5I) ARNICA MONTANA (UNII: O80TY208ZW) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) ALCOHOL (UNII: 3K9958V90M) METHYL GLUCOSE DIOLEATE (UNII: FA9KFJ4Z6P) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72683-002-01 1 in 1 CARTON 01/21/2019 1 85 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 01/21/2019 Labeler - Proximity Capital Partners LLC dba Asutra (081214985) Establishment Name Address ID/FEI Business Operations BioLyte Laboratories, LLC 015560564 manufacture(72683-002)