NDC 72394-000 Clean
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 72394-000?
What are the uses for Clean?
Which are Clean UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Clean 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:
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- LEVOMENOL (UNII: 24WE03BX2T)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- CHAMOMILE (UNII: FGL3685T2X)
- ORANGE (UNII: 5EVU04N5QU)
- ORANGE PEEL (UNII: TI9T76XD44)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ISODODECANE (UNII: A8289P68Y2)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- DULSE (UNII: 7832HOY4ZQ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPANEDIOL (UNII: 5965N8W85T)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[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".