NDC 36800-042 Pain Relief Rub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36800 - Topco Associates Llc
- 36800-042 - Pain Relief Rub
Product Packages
NDC Code 36800-042-04
Package Description: 1 TUBE in 1 BOX / 114 g in 1 TUBE
Product Details
What is NDC 36800-042?
What are the uses for Pain Relief Rub?
Which are Pain Relief Rub UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- MENTHYL SALICYLATE, (+/-)- (UNII: 43XOA705ZD)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Pain Relief Rub 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 940 (UNII: 4Q93RCW27E)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- WATER (UNII: 059QF0KO0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Pain Relief Rub?
- RxCUI: 283083 - camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical Cream
- RxCUI: 283083 - camphor 40 MG/ML / menthol 100 MG/ML / methyl salicylate 300 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".