NDC 59062-1304 Babyganics Eczema
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59062-1304?
What are the uses for Babyganics Eczema?
Which are Babyganics Eczema UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Babyganics Eczema 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)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- COCOA BUTTER (UNII: 512OYT1CRR)
- OAT (UNII: Z6J799EAJK)
- NIGELLA SATIVA SEED OIL (UNII: CS4U38E731)
- CARROT SEED OIL (UNII: 595AO13F11)
- CHIA SEED OIL (UNII: MC2LH51BO7)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- CRANBERRY SEED OIL (UNII: 73KDS3BW5E)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- TOCOPHEROL (UNII: R0ZB2556P8)
- GLYCERYL DILAURATE (UNII: MFL3ZIE8SK)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM HYDROXYMETHYLGLYCINATE (UNII: DIG6BWZ9XT)
What is the NDC to RxNorm Crosswalk for Babyganics Eczema?
- 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".