Valtrum Analgesic

Product NDC
75849-312
11-digit product format
758490312
Labeler code
75849
Product ID
75849-312_c9ed6773-b657-720c-e053-2a95a90ae2b1
Type
HUMAN OTC DRUG
Nonproprietary name
CAMPHOR (SYNTHETIC), MENTHOL, MENTHYL SALICYLATE
Dosage form
GEL
Route
TOPICAL
Labeler
Laboratorios Quantium LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-07-15
Marketing end
0000-00-00
Substance
CAMPHOR (SYNTHETIC); MENTHOL; MENTHYL SALICYLATE, (+/-)-
Active strength
30 mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75849-312-032023-01-30C16284748780-1f386c649-d7d1-0266-e053-dadaa90a7c1aValtrum Topical Analgesic Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75849-312-03Valtrum Analgesic90 g in 1 TUBEGEL903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75849-312VALTRUM ANALGESIC (CAMPHOR (SYNTHETIC), MENTHOL, MENTHYL SALICYLATE) GEL [LABORATORIOS QUANTIUM LLC]3Legacy NDC, 1 package rows20210820_c72e768c-d1ee-ba0b-e053-2a95a90a5f99.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2123377camphor 3 % / menthol 3 % / methyl salicylate 10 % Topical GelPSNc72e768c-d1ee-ba0b-e053-2a95a90a5f993
2123377camphor 0.03 MG/MG / menthol 0.03 MG/MG / methyl salicylate 0.1 MG/MG Topical GelSCDc72e768c-d1ee-ba0b-e053-2a95a90a5f993
2123377camphor 3 % / menthol 3 % / methyl salicylate 10 % Topical GelSYc72e768c-d1ee-ba0b-e053-2a95a90a5f993

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
75849-312-037584903120390 g in 1 TUBE (75849-312-03) 90 g2021-07-150000-00-00NoNoCurrent