NDC 61625-689 Piranha Brand Foaming Antibacterial Hand
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What is NDC 61625-689?
What are the uses for Piranha Brand Foaming Antibacterial Hand?
Which are Piranha Brand Foaming Antibacterial Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Piranha Brand Foaming Antibacterial Hand 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)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- EDETATE SODIUM (UNII: MP1J8420LU)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ISOSTEARAMIDOPROPYL MORPHOLINE LACTATE (UNII: 082Y3WQI5K)
What is the NDC to RxNorm Crosswalk for Piranha Brand Foaming Antibacterial Hand?
- RxCUI: 413247 - triclosan 0.5 % Medicated Liquid Soap
- RxCUI: 413247 - triclosan 5 MG/ML Medicated Liquid Soap
- RxCUI: 413247 - triclosan 0.5 % Foaming Medicated Hand 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".