NDC 72275-702 Diclovix
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 72275-702?
What are the uses for Diclovix?
Which are Diclovix UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Diclovix 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:
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)
- METHYL ACRYLATE (UNII: WC487PR91H)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- NONOXYNOL-30 (UNII: JJX07DG188)
- STARCH, CORN (UNII: O8232NY3SJ)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ACRYLIC ACID (UNII: J94PBK7X8S)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Diclovix?
- RxCUI: 2287556 - camphor 2 % / lidocaine 2.5 % / methyl salicylate 4 % Medicated Patch
- RxCUI: 2287556 - camphor 0.02 MG/MG / lidocaine 0.025 MG/MG / methyl salicylate 0.04 MG/MG Medicated Patch
- RxCUI: 857700 - diclofenac sodium 1.5 % Topical Solution
- RxCUI: 857700 - diclofenac sodium 15 MG/ML Topical Solution
- RxCUI: 857700 - diclofenac sodium 1.5 % (as diclofenac sodium 16.05 MG/ML) Topical Solution
* 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".