NDC 49035-805 Island Spring Antibacterial Body Wash With Moisturizers
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49035-805?
What are the uses for Island Spring Antibacterial Body Wash With Moisturizers?
Which are Island Spring Antibacterial Body Wash With Moisturizers UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Island Spring Antibacterial Body Wash With Moisturizers 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYETHYLENE GLYCOL 900 (UNII: UEP843BRCQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- ISOSTEARAMIDOPROPYL MORPHOLINE LACTATE (UNII: 082Y3WQI5K)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
What is the NDC to RxNorm Crosswalk for Island Spring Antibacterial Body Wash With Moisturizers?
- RxCUI: 1020118 - triclosan 0.15 % Medicated Liquid Soap
- RxCUI: 1020118 - triclosan 1.5 MG/ML Medicated Liquid 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".