NDC 69842-962 Cvs Health Eczema Skin Relief Skin Protectant
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What is NDC 69842-962?
What are the uses for Cvs Health Eczema Skin Relief Skin Protectant?
Which are Cvs Health Eczema Skin Relief Skin Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Cvs Health Eczema Skin Relief Skin Protectant 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PROPANEDIOL (UNII: 5965N8W85T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- PETROLATUM (UNII: 4T6H12BN9U)
- EDETATE SODIUM (UNII: MP1J8420LU)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- OAT (UNII: Z6J799EAJK)
- SHEA BUTTER (UNII: K49155WL9Y)
- GINGER (UNII: C5529G5JPQ)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PANTHENOL (UNII: WV9CM0O67Z)
- CERAMIDE NP (UNII: 4370DF050B)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- LEVOMENOL (UNII: 24WE03BX2T)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Cvs Health Eczema Skin Relief Skin Protectant?
- RxCUI: 1591951 - colloidal oatmeal 2 % Topical Lotion
- RxCUI: 1591951 - colloidal oatmeal 20 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".