NDC 79804-260 Pain Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 79804-260?
What are the uses for Pain Cream?
Which are Pain Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Pain Cream 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:
- CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- JOJOBA OIL (UNII: 724GKU717M)
- LAURETH-7 (UNII: Z95S6G8201)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SHEA BUTTER (UNII: K49155WL9Y)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- SPEARMINT OIL (UNII: C3M81465G5)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Pain Cream?
- RxCUI: 2610119 - camphor 5 % / menthol 6 % Topical Cream
- RxCUI: 2610119 - camphor 50 MG/ML / menthol 60 MG/ML Topical Cream
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[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".