NDC 43493-0001 Pain Relief Rub Iampur
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43493-0001?
What are the uses for Pain Relief Rub Iampur?
Which are Pain Relief Rub Iampur UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Pain Relief Rub Iampur 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA (UNII: O80TY208ZW)
- RICE BRAN OIL (UNII: LZO6K1506A)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
What is the NDC to RxNorm Crosswalk for Pain Relief Rub Iampur?
- RxCUI: 1368275 - camphor 4 % / menthol 4 % / methyl salicylate 11 % Topical Cream
- RxCUI: 1368275 - camphor 40 MG/ML / menthol 40 MG/ML / methyl salicylate 110 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".