NDC 58503-055 Xtracare With Cooling Action Oatmeal Skin Relief Calmin
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What is NDC 58503-055?
What are the uses for Xtracare With Cooling Action Oatmeal Skin Relief Calmin?
Which are Xtracare With Cooling Action Oatmeal Skin Relief Calmin UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Xtracare With Cooling Action Oatmeal Skin Relief Calmin 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- OAT (UNII: Z6J799EAJK)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MENTHOL (UNII: L7T10EIP3A)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Xtracare With Cooling Action Oatmeal Skin Relief Calmin?
- RxCUI: 891710 - dimethicone 1.3 % Topical Lotion
- RxCUI: 891710 - dimethicone 13 MG/ML Topical Lotion
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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".