NDC 45765-5100 Baby Magic Medicated Patty Cake
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 45765 - Naterra International Inc.
- 45765-5100 - Baby Magic Medicated Patty Cake
Product Packages
NDC Code 45765-5100-0
Package Description: 11 g in 1 TRAY
Product Details
What is NDC 45765-5100?
What are the uses for Baby Magic Medicated Patty Cake?
Which are Baby Magic Medicated Patty Cake 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 Baby Magic Medicated Patty Cake 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:
- ALLANTOIN (UNII: 344S277G0Z)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CANDELILLA WAX (UNII: WL0328HX19)
- GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
- HEXYL DECANOATE (UNII: D2D42X538B)
- LAUROYL LYSINE (UNII: 113171Q70B)
- NYLON-12 (UNII: 446U8J075B)
What is the NDC to RxNorm Crosswalk for Baby Magic Medicated Patty Cake?
- RxCUI: 1146020 - zinc oxide 28 % Topical Cream
- RxCUI: 1146020 - zinc oxide 280 MG/ML Topical Cream
- RxCUI: 1146020 - ZNO 280 MG/ML Topical Cream
- RxCUI: 1246906 - Baby Magic Patty Cake 28 % Topical Cream
- RxCUI: 1246906 - zinc oxide 280 MG/ML Topical Cream [Patty Cake]
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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".