NDC 69740-492 Dermal Wound Cleanser
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What is NDC 69740-492?
What are the uses for Dermal Wound Cleanser?
Which are Dermal Wound Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Dermal Wound Cleanser 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
What is the NDC to RxNorm Crosswalk for Dermal Wound Cleanser?
- RxCUI: 582205 - benzethonium chloride 0.13 % Topical Spray
- RxCUI: 582205 - benzethonium chloride 1.3 MG/ML Topical Spray
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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".