Label: EMU THERAPY RED HOT PEPPER PAIN RELIEF CREAM- menthol, capsaicin cream
- NDC Code(s): 83591-417-00
- Packager: ACA MANAGEMENT LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 6, 2023
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- Active Ingredient:
- Uses:
- Warnings:
- Directions:
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Inactive Ingredients:
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Anthemis Nobilis (Roman Chamomile) Oil, Aqua (Deionized Water), Arnica Montana Flower Extract, Ascorbyl Palmitate (Vitamin C), Calendula Officinalis Extract, Centaurea Cyanus (Corniflower) Extract, Chamomilla Recutita (Chamomile) Extract, Coriandrum Sativum (Coriander) Oil, Emu Oil, Ethylhexylglycerin, Hamamelis Virginiana (Witch Hazel), Helianthus Annuus (Sunflower) Oil, Hypericum Perforatum (St. John's Wort), Lamium Album (White Nettle) Extract, Methylsulfonyl Methane (MSM), Parfum (Fragrance), Phenoxyethanol, Salix Alba (Willow) Bark Extract, SD-Alcohol 40B, Sodium Lauryl Sulfate, Sorbitol, Tillia Cordata (Linden) Bark Extract, Triethanolamine, Fever Few Extract, FD&C Blue #1, FD&C Yellow #5.
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INGREDIENTS AND APPEARANCE
EMU THERAPY RED HOT PEPPER PAIN RELIEF CREAM
menthol, capsaicin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83591-417 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 15 mg in 1 mL CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.25 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ASCORBYL PALMITATE (UNII: QN83US2B0N) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CHAMOMILE (UNII: FGL3685T2X) CORIANDER (UNII: 1OV56052IK) EMU OIL (UNII: 344821WD61) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) LAMIUM ALBUM WHOLE (UNII: 046Y1357I6) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PHENOXYETHANOL (UNII: HIE492ZZ3T) SALIX ALBA BARK (UNII: 205MXS71H7) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SORBITOL (UNII: 506T60A25R) TROLAMINE (UNII: 9O3K93S3TK) TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K) 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:83591-417-00 237 mL in 1 JAR; Type 0: Not a Combination Product 08/08/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/08/2023 Labeler - ACA MANAGEMENT LLC (119034214)