NDC 66267-976 Ear Wax Removal Drops
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What is NDC 66267-976?
What are the uses for Ear Wax Removal Drops?
Which are Ear Wax Removal Drops UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBAMIDE PEROXIDE (UNII: 31PZ2VAU81)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V) (Active Moiety)
Which are Ear Wax Removal Drops 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TARTARIC ACID (UNII: W4888I119H)
What is the NDC to RxNorm Crosswalk for Ear Wax Removal Drops?
- RxCUI: 702050 - carbamide peroxide 6.5 % Otic Solution
- RxCUI: 702050 - carbamide peroxide 65 MG/ML Otic Solution
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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".