NDC 52410-8038 Ameriwash
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 52410-8038?
What are the uses for Ameriwash?
Which are Ameriwash UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Ameriwash 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ALCOHOL (UNII: 3K9958V90M)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
- WATER (UNII: 059QF0KO0R)
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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".