NDC 21695-222 Acetic Acid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-222 - Acetic Acid
Product Packages
NDC Code 21695-222-15
Package Description: 1 BOTTLE in 1 BOX / 15 mL in 1 BOTTLE
Product Details
What is NDC 21695-222?
What are the uses for Acetic Acid?
Which are Acetic Acid UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETIC ACID (UNII: Q40Q9N063P)
- ACETIC ACID (UNII: Q40Q9N063P) (Active Moiety)
Which are Acetic Acid 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- PROPYLENE GLYCOL DIACETATE (UNII: 5Z492UNF9O)
- SODIUM ACETATE (UNII: 4550K0SC9B)
What is the NDC to RxNorm Crosswalk for Acetic Acid?
- RxCUI: 197305 - acetic acid 2 % Otic Solution
- RxCUI: 197305 - acetic acid 20 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".