NDC 68196-804 Antibacterial Sparkling Mist
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What is NDC 68196-804?
What are the uses for Antibacterial Sparkling Mist?
Which are Antibacterial Sparkling Mist UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Antibacterial Sparkling Mist 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)
- PEG-8 DIOLEATE (UNII: 6JR5A7273E)
- GLYCERIN (UNII: PDC6A3C0OX)
- INDELOXAZINE HYDROCHLORIDE (UNII: 15QZ6NE84E)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- NIACINAMIDE (UNII: 25X51I8RD4)
- HIBISCUS SABDARIFFA FLOWER (UNII: 45TGG6IU6M)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- EDETATE SODIUM (UNII: MP1J8420LU)
- GINGER (UNII: C5529G5JPQ)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Antibacterial Sparkling Mist?
- 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".