NDC 64058-155 Miracle Plus Overnight Pain Relieving
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What is NDC 64058-155?
What are the uses for Miracle Plus Overnight Pain Relieving?
Which are Miracle Plus Overnight Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Miracle Plus Overnight Pain Relieving Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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)
What is the NDC to RxNorm Crosswalk for Miracle Plus Overnight Pain Relieving?
- RxCUI: 1373385 - Capsicum oleoresin 0.0625 % Topical Gel
- RxCUI: 1373385 - Capsicum oleoresin 0.000625 MG/MG Topical Gel
- RxCUI: 1373385 - Capsicum oleoresin 0.0625 % (capsaicin 0.025 % ) Topical Gel
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".