Label: AMP RELIEF PAIN RELIEF CREAM- menthol cream
- NDC Code(s): 82560-283-00
- Packager: COASTAL FORMULAS LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 11, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses:
-
Warnings:
For external use only.
Stop use and ask a doctor if
- rash or irritation develops and lasts
- condition worsens
- sysmptoms persist for more than 7 days
- clears up and occurs again within a few days
- Directions:
- Flammable:
-
Inactive ingredients:
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, Isopropyl Myristate, Methyl Salicylate, Paraffinum Liquidum, Phenoxyethanol, Polysorbate-80, SD-Alcohol 40B, Triethanolamine, FD& C Blue #1, FD&C Yellow #5
- Questions?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
AMP RELIEF PAIN RELIEF CREAM
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82560-283 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 80 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EUCALYPTUS OIL (UNII: 2R04ONI662) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) METHYL SALICYLATE (UNII: LAV5U5022Y) MINERAL OIL (UNII: T5L8T28FGP) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYSORBATE 80 (UNII: 6OZP39ZG8H) TROLAMINE (UNII: 9O3K93S3TK) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82560-283-00 3939.19 mL in 1 JUG; Type 0: Not a Combination Product 03/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 03/25/2022 Labeler - COASTAL FORMULAS LLC (085954368)