NDC 76347-125 Anti-chafe Stick Pro Series
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76347-125?
What are the uses for Anti-chafe Stick Pro Series?
Which are Anti-chafe Stick Pro Series UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Anti-chafe Stick Pro Series 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:
- HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CANDELILLA WAX (UNII: WL0328HX19)
- CERESIN (UNII: Q1LS2UJO3A)
- TALC (UNII: 7SEV7J4R1U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SHEA BUTTER (UNII: K49155WL9Y)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
- CRANBERRY SEED OIL (UNII: 73KDS3BW5E)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
What is the NDC to RxNorm Crosswalk for Anti-chafe Stick Pro Series?
- RxCUI: 1044541 - allantoin 0.5 % Topical Ointment
- RxCUI: 1044541 - allantoin 0.005 MG/MG Topical Ointment
- RxCUI: 1044541 - allantoin 0.5 % Topical Stick
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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".