NDC 58443-0223 Eternal Spirit Beauty Painless Pain Relieving Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58443-0223?
What are the uses for Eternal Spirit Beauty Painless Pain Relieving Cream?
Which are Eternal Spirit Beauty Painless Pain Relieving Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Eternal Spirit Beauty Painless Pain Relieving Cream 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:
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- SHEA BUTTER (UNII: K49155WL9Y)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TEA TREE OIL (UNII: VIF565UC2G)
- CHOLINE BITARTRATE (UNII: 6K2W7T9V6Y)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MINERAL OIL (UNII: T5L8T28FGP)
- PYRIDOXINE (UNII: KV2JZ1BI6Z)
- TROLAMINE (UNII: 9O3K93S3TK)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- WATER (UNII: 059QF0KO0R)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LICORICE (UNII: 61ZBX54883)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)
What is the NDC to RxNorm Crosswalk for Eternal Spirit Beauty Painless Pain Relieving Cream?
- RxCUI: 416982 - menthol 1.25 % Topical Cream
- RxCUI: 416982 - menthol 12.5 MG/ML Topical Cream
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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".