NDC 75849-100 Valtrum Us Soothing Topical Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75849 - Laboratorios Quantium Llc
- 75849-100 - Valtrum Us Soothing Topical Analgesic
Product Packages
NDC Code 75849-100-00
Package Description: 90 g in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 75849-100?
What are the uses for Valtrum Us Soothing Topical Analgesic?
Which are Valtrum Us 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)
Which are Valtrum Us 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)
- ARNICA MONTANA (UNII: O80TY208ZW)
- CAT'S CLAW (UNII: 9060PRM18Q)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Valtrum Us Soothing Topical Analgesic?
- RxCUI: 1045376 - camphor 3 % / menthol 3 % Topical Ointment
- RxCUI: 1045376 - camphor 0.03 MG/MG / menthol 0.03 MG/MG Topical Ointment
- RxCUI: 1092556 - Valtrum 3 % / 3 % Topical Ointment
- RxCUI: 1092556 - camphor 0.03 MG/MG / menthol 0.03 MG/MG Topical Ointment [Valtrum]
- RxCUI: 1092556 - Valtrum (camphor 3 % / menthol 3 % ) 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".