NDC 42957-001 Babyspa Shea Butter Diaper
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42957-001?
What are the uses for Babyspa Shea Butter Diaper?
Which are Babyspa Shea Butter Diaper 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 Babyspa Shea Butter Diaper 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:
- SHEA BUTTER (UNII: K49155WL9Y)
- ALOE VERA FLOWER (UNII: 575DY8C1ER)
- COCOA BUTTER (UNII: 512OYT1CRR)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- STARCH, POTATO (UNII: 8I089SAH3T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- KAOLIN (UNII: 24H4NWX5CO)
- SESAME OIL (UNII: QX10HYY4QV)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CALENDULA OFFICINALIS SEED OIL (UNII: 9JS8DS42SV)
- WATER (UNII: 059QF0KO0R)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- EPIGALLOCATECHIN GALLATE (UNII: BQM438CTEL)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- GLYCERIN (UNII: PDC6A3C0OX)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- BORAGE OIL (UNII: F8XAG1755S)
- OENOTHERA BIENNIS (UNII: 76UI55V071)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
What is the NDC to RxNorm Crosswalk for Babyspa Shea Butter Diaper?
- RxCUI: 417994 - zinc oxide 12 % Topical Cream
- RxCUI: 417994 - zinc oxide 120 MG/ML Topical Cream
- RxCUI: 417994 - ZNO 120 MG/ML Topical Cream
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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".