NDC 21695-707 Flector
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 21695-707?
What are the uses for Flector?
Which are Flector UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC EPOLAMINE (UNII: X5F8EKL9ZG)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
Which are Flector 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SORBITOL (UNII: 506T60A25R)
- GELATIN (UNII: 2G86QN327L)
- KAOLIN (UNII: 24H4NWX5CO)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Flector?
- RxCUI: 855626 - diclofenac epolamine 1.3 % Twice-Daily Medicated Patch
- RxCUI: 855626 - Twice-Daily diclofenac epolamine 0.013 MG/MG Medicated Patch
- RxCUI: 855628 - Flector 1.3 % Twice-Daily Medicated Patch
- RxCUI: 855628 - Twice-Daily diclofenac epolamine 0.013 MG/MG Medicated Patch [Flector]
- RxCUI: 855628 - Twice-Daily Flector 0.013 MG/MG Medicated Patch
* Please review the disclaimer below.
[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".