Home NDC 75849-301 Valtrum Topical Analgesic Roll On
Product NDC 75849-301
11-digit product format 758490301
Labeler code 75849
Product ID 75849-301_e0089b62-e19a-4ab7-a2f0-a8e9a70ff2e8
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID MENTHOL CAMPHOR (NATURAL)
Dosage form GEL
Route TOPICAL
Labeler LABORATORIOS QUANTIUM LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-01
Substance METHYL SALICYLATE; MENTHOL, UNSPECIFIED FORM; CAMPHOR (NATURAL)
Active strength 10; 3; 3 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Valtrum Topical Analgesic Roll On
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHYL SALICYLATE 10 g/100g MENTHOL, UNSPECIFIED FORM 3 g/100g CAMPHOR (NATURAL) 3 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination LAV5U5022Y Internal UNII lookup L7T10EIP3A Internal UNII lookup N20HL7Q941 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2123377 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 75849-301-03 Valtrum Topical Analgesic Roll On 90 g in 1 TUBE, WITH APPLICATOR GEL 90 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75849-301 VALTRUM TOPICAL ANALGESIC ROLL ON (SALICYLIC ACID MENTHOL CAMPHOR (NATURAL)) GEL [LABORATORIOS QUANTIUM LLC] 3 Current NDC, Legacy NDC, 1 package rows 20231129_28167e2a-9afb-44e7-90c7-9577df9504b6.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 97 of 151 · 3,010 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 75849-301-03 75849030103 90 g in 1 TUBE, WITH APPLICATOR (75849-301-03) 90 g 2019-03-01 0000-00-00 No No Current