NDC 51209-010 Dalan Antibacterial Deodorant Ocean Breeze
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51209-010?
What are the uses for Dalan Antibacterial Deodorant Ocean Breeze?
Which are Dalan Antibacterial Deodorant Ocean Breeze UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Dalan Antibacterial Deodorant Ocean Breeze 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:
- SODIUM PALMATE (UNII: S0A6004K3Z)
- WATER (UNII: 059QF0KO0R)
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ETIDRONIC ACID (UNII: M2F465ROXU)
- DISODIUM DISTYRYLBIPHENYL DISULFONATE (UNII: 81G7704MYR)
- C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- GERANIOL (UNII: L837108USY)
- CITRAL (UNII: T7EU0O9VPP)
What is the NDC to RxNorm Crosswalk for Dalan Antibacterial Deodorant Ocean Breeze?
- RxCUI: 252551 - triclosan 0.1 % Medicated Bar Soap
- RxCUI: 252551 - triclosan 0.001 MG/MG Medicated Bar Soap
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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".