NDC 72275-734 Diclovix Cm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72275 - Primary Pharmaceuticals, Inc
- 72275-734 - Diclovix Cm
Product Characteristics
Product Packages
NDC Code 72275-734-77
Package Description: 1 KIT in 1 KIT * 5.6 mL in 1 PACKET (53329-984-16) * 60 g in 1 TUBE * 150 mL in 1 BOTTLE (52565-002-05)
Product Details
What is NDC 72275-734?
What are the uses for Diclovix Cm?
Which are Diclovix Cm UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Diclovix Cm 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)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEPPERMINT (UNII: V95R5KMY2B)
- HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ACETATE (UNII: 4Q43814HXS)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PPG-20 METHYL GLUCOSE ETHER DISTEARATE (UNII: 0057334FAB)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARETH-100 (UNII: 4OH5W9UM87)
What is the NDC to RxNorm Crosswalk for Diclovix Cm?
- RxCUI: 198555 - capsaicin 0.025 % Topical Cream
- RxCUI: 198555 - capsaicin 0.25 MG/ML Topical Cream
- RxCUI: 2119857 - ActivICE 8 % Topical Gel
- RxCUI: 2119857 - menthol 0.08 MG/MG Topical Gel [ActivICE]
- RxCUI: 2119857 - ActivICE 0.08 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".