Label: PR- menthol lotion
- NDC Code(s): 72358-101-03, 72358-101-04
- Packager: Amphp, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 4, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Shake well. 15 minutes to 2 hours before your workout, apply generously to the muscles you use most (30 minutes before water sports). Completely cover each muscle, a palmful per use. Reapply after for added recovery. Wash hands.
Adults and children 2 years of age or older: apply to affected area not more than 3 to 4 times daily
Children under 2 years of age: consult a doctor
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- PR Lotion 300 gram tube principal display panel
- PR Lotion 20 gram packet principal display panel
- PR Lotion 100 gram tube principal display panel
-
INGREDIENTS AND APPEARANCE
PR
menthol lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72358-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.5 g in 100 g Inactive Ingredients Ingredient Name Strength JOJOBA OIL (UNII: 724GKU717M) POLYGLYCERYL-3 LAURATE (UNII: Y9ZSR39D0E) WATER (UNII: 059QF0KO0R) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) COCONUT OIL (UNII: Q9L0O73W7L) SODIUM BICARBONATE (UNII: 8MDF5V39QO) ALCOHOL (UNII: 3K9958V90M) BENZYL ALCOHOL (UNII: LKG8494WBH) HYDRATED SILICA (UNII: Y6O7T4G8P9) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLOXAMER 407 (UNII: TUF2IVW3M2) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72358-101-04 300 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/01/2018 2 NDC:72358-101-03 20 g in 1 PACKET; Type 0: Not a Combination Product 11/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/01/2018 Labeler - Amphp, Inc (081138140)