NDC 59779-451 3-in-1 Relief Cvs
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs
- 59779-451 - 3-in-1 Relief
Product Packages
NDC Code 59779-451-05
Package Description: 170 g in 1 BOTTLE
Product Details
What is NDC 59779-451?
What are the uses for 3-in-1 Relief Cvs?
Which are 3-in-1 Relief Cvs UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are 3-in-1 Relief Cvs 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)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- PETROLATUM (UNII: 4T6H12BN9U)
- PANTHENOL (UNII: WV9CM0O67Z)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- OAT KERNEL OIL (UNII: 3UVP41R77R)
- OAT (UNII: Z6J799EAJK)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CUCUMBER (UNII: YY7C30VXJT)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHAMOMILE (UNII: FGL3685T2X)
- CERAMIDE NP (UNII: 4370DF050B)
- SORBITOL (UNII: 506T60A25R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- OLEIC ACID (UNII: 2UMI9U37CP)
- FERROUS OXIDE (UNII: G7036X8B5H)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARETH-20 (UNII: L0Q8IK9E08)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- 4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
What is the NDC to RxNorm Crosswalk for 3-in-1 Relief Cvs?
- RxCUI: 240464 - colloidal oatmeal 1 % Topical Lotion
- RxCUI: 240464 - colloidal oatmeal 10 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".