NDC 51141-0237 Atopalm Diaper Rash
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51141-0237?
What are the uses for Atopalm Diaper Rash?
Which are Atopalm Diaper Rash UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Atopalm Diaper Rash 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)
- PETROLATUM (UNII: 4T6H12BN9U)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- WHITE WAX (UNII: 7G1J5DA97F)
- TALC (UNII: 7SEV7J4R1U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MYRISTOYL/PALMITOYL OXOSTEARAMIDE/ARACHAMIDE MEA (UNII: 1211AIM8G7)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- PANTHENOL (UNII: WV9CM0O67Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Atopalm Diaper Rash?
- RxCUI: 1299027 - ATOPALM Diaper Rash 10 % Topical Cream
- RxCUI: 1299027 - zinc oxide 100 MG/ML Topical Cream [Atopalm Diaper Rash]
- RxCUI: 1299027 - Atopalm Diaper Rash 10 % Topical Cream
- RxCUI: 1299027 - Atopalm Diaper Rash 100 MG/ML Topical Cream
- RxCUI: 1299027 - ZNO 100 MG/ML Topical Cream [Atopalm Diaper Rash]
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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".