NDC 50090-4021 Diclofenac Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 50090-4021?
What are the uses for Diclofenac Sodium?
Which are Diclofenac Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
Which are Diclofenac Sodium 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:
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- AMMONIA (UNII: 5138Q19F1X)
What is the NDC to RxNorm Crosswalk for Diclofenac Sodium?
- RxCUI: 855633 - diclofenac sodium 1 % Topical Gel
- RxCUI: 855633 - diclofenac sodium 0.01 MG/MG Topical Gel
* Please review the disclaimer below.
Patient Education
Diclofenac Topical (actinic keratosis)
Diclofenac topical gel (Solaraze) is used to treat actinic keratosis (flat, scaly growths on the skin caused by too much sun exposure). Diclofenac is in a class of medications called nonsteroidal anti-inflammatory drugs (NSAIDs). The way diclofenac gel works to treat actinic keratosis is not known. Diclofenac is also available as a liquid (Pennsaid) and a gel (Voltaren) that are applied to the skin to treat arthritis pain. This monograph only gives information about diclofenac gel (Solaraze) for actinic keratosis. If you are using either of the products for osteoarthritis, read the monograph entitled diclofenac topical (osteoarthritis pain).
[Learn More]
* 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".