NDC 42387-135 Grahams Natural Diaper Rash
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What is NDC 42387-135?
What are the uses for Grahams Natural Diaper Rash?
Which are Grahams Natural 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 Grahams Natural 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:
- JOJOBA OIL (UNII: 724GKU717M)
- CHAMOMILE (UNII: FGL3685T2X)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- WATER (UNII: 059QF0KO0R)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- ALMOND OIL (UNII: 66YXD4DKO9)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- SHEA BUTTER (UNII: K49155WL9Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CALENDULA ARVENSIS LEAF (UNII: 3U3U118F2L)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- SODIUM LEVULINATE (UNII: VK44E1MQU8)
What is the NDC to RxNorm Crosswalk for Grahams Natural Diaper Rash?
- 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".