Label: MIRACLE PLUS OVERNIGHT PAIN RELIEVING- capsaicin gel
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Contains inactivated NDC Code(s)
NDC Code(s): 64058-155-42, 64058-155-44 - Packager: Concept Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 3, 2014
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
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Other information
- It is recommended to test for skin sensitivity prior to use. Apply product to a small area, follow the directions and wait 24 hours. Proceed with application if no adverse reaction.
- A burning sensation may occur upon initial application but generally disappears with continued use. For a severe burning discomfort, remove excess product with a soft cloth and cooking oil.
- If applying product to hands, wait 30 minutes before washing.
- Avoid water, heat, or direct sunlight while using product.
- If wearing contact lenses, insert prior to application and avoid touching them after applying product.
- If eye contact occurs, flush immediately with water.
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Inactive ingredients
Water (Aqua), Glycerin, PEG-75 Lanolin, Aloe Barbadensis Leaf Juice, PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Polysorbate 20, Glucosamine HCI, Emu Oil, Dimethyl Sulfone, Celosia Argentea Seed Extract, Ginkgo Biloba Extract, Panax Ginseng Root Extract, Medicago Sativa (Alfalfa) Extract, Cymbopogon Schoenanthus Extract, Tocopheryl Acetate, DMDM Hydantoin, Propylene Glycol, Methylparaben, Propylparaben.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 113 g Bottle Label
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INGREDIENTS AND APPEARANCE
MIRACLE PLUS OVERNIGHT PAIN RELIEVING
capsaicin gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64058-155 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Capsaicin (UNII: S07O44R1ZM) (Capsaicin - UNII:S07O44R1ZM) Capsaicin 0.02825 g in 113 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) PEG-75 LANOLIN (UNII: 09179OX7TB) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALFALFA LEAF (UNII: HY3L927V6M) CYMBOPOGON SCHOENANTHUS LEAF (UNII: XF54B1Z2HF) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) GINKGO (UNII: 19FUJ2C58T) POLYSORBATE 20 (UNII: 7T1F30V5YH) EMU OIL (UNII: 344821WD61) DMDM HYDANTOIN (UNII: BYR0546TOW) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) ASIAN GINSENG (UNII: CUQ3A77YXI) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64058-155-44 113 g in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:64058-155-42 57 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part348 11/20/2014 Labeler - Concept Laboratories, Inc. (962282612) Establishment Name Address ID/FEI Business Operations Concept Laboratories, Inc. 962282612 MANUFACTURE(64058-155)