NDC 0164-2207 White Mallow Diaper Rash Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 0164-2207?
What are the uses for White Mallow Diaper Rash Cream?
Which are White Mallow Diaper Rash Cream 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 White Mallow Diaper Rash Cream 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:
- BORAGE OIL (UNII: F8XAG1755S)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- GLYCERIN (UNII: PDC6A3C0OX)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- LACTIC ACID (UNII: 33X04XA5AT)
- LANOLIN (UNII: 7EV65EAW6H)
- SESAME OIL (UNII: QX10HYY4QV)
- SODIUM CAPROYL LACTYLATE (UNII: 87WR3BHC09)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALMOND OIL (UNII: 66YXD4DKO9)
- VIOLA TRICOLOR (UNII: 9Q24RAI43V)
- WATER (UNII: 059QF0KO0R)
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
- WHITE WAX (UNII: 7G1J5DA97F)
What is the NDC to RxNorm Crosswalk for White Mallow Diaper Rash Cream?
- RxCUI: 1546589 - zinc oxide 14 % Topical Cream
- RxCUI: 1546589 - zinc oxide 140 MG/ML Topical Cream
- RxCUI: 1546589 - ZNO 140 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".