NDC 54868-5965 Voltaren
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5965 - Voltaren
Product Packages
NDC Code 54868-5965-0
Package Description: 1 TUBE in 1 CARTON / 100 g in 1 TUBE
Product Details
What is NDC 54868-5965?
What are the uses for Voltaren?
Which are Voltaren UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
Which are Voltaren 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:
- AMMONIA (UNII: 5138Q19F1X)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Voltaren?
- RxCUI: 855633 - diclofenac sodium 1 % Topical Gel
- RxCUI: 855633 - diclofenac sodium 0.01 MG/MG Topical Gel
- RxCUI: 855635 - Voltaren 1 % Topical Gel
- RxCUI: 855635 - diclofenac sodium 0.01 MG/MG Topical Gel [Voltaren]
- RxCUI: 855635 - Voltaren 0.01 MG/MG Topical Gel
* 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".