NDC 75849-300 Valtrum Soothing Topical Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75849 - Laboratorios Quantium Llc
- 75849-300 - Valtrum Soothing Topical Analgesic
Product Packages
NDC Code 75849-300-00
Package Description: 1 BOTTLE in 1 CARTON / 90 g in 1 BOTTLE
Product Details
What is NDC 75849-300?
What are the uses for Valtrum Soothing Topical Analgesic?
Which are Valtrum Soothing Topical Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Valtrum Soothing Topical Analgesic 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:
- ALCOHOL (UNII: 3K9958V90M)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Valtrum Soothing Topical Analgesic?
- RxCUI: 1721696 - camphor 2.5 % / menthol 2.5 % / methyl salicylate 10 % Topical Ointment
- RxCUI: 1721696 - camphor 0.025 MG/MG / menthol 0.025 MG/MG / methyl salicylate 0.1 MG/MG Topical Ointment
- RxCUI: 1721701 - Valtrum Soothing 2.5 % / 2.5 % / 10 % Topical Ointment
- RxCUI: 1721701 - camphor 0.025 MG/MG / menthol 0.025 MG/MG / methyl salicylate 0.1 MG/MG Topical Ointment [Valtrum Soothing]
- RxCUI: 1721701 - Valtrum Soothing (camphor 2.5 % / menthol 2.5 % / methyl salicylate 10 % ) Topical Ointment
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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".