Home NDC 71262-008 Liberdol Topical Analgesic
Product NDC 71262-008
11-digit product format 712620008
Labeler code 71262
Product ID 71262-008_0b6df7b0-af6a-e3df-e063-6394a90ad193
Type HUMAN OTC DRUG
Nonproprietary name METHYL SALICYLATE, MENTHOL, CAMPHOR (SYNTHETIC)
Dosage form SPRAY
Route TOPICAL
Labeler ViaDerma Distribution, Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-01
Substance METHYL SALICYLATE; MENTHOL; CAMPHOR (SYNTHETIC)
Active strength 300; 100; 40 mg/mL; mg/mL; mg/mL
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 Liberdol Topical Analgesic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHYL SALICYLATE 300 mg/mL MENTHOL 100 mg/mL CAMPHOR (SYNTHETIC) 40 mg/mL
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 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1600127 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71262-008-55 Liberdol Topical Analgesic 1 in 1 CARTON SPRAY 1 2 71262-008-55 Liberdol Topical Analgesic 55 mL in 1 BOTTLE SPRAY 55 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71262-008 LIBERDOL TOPICAL ANALGESIC (METHYL SALICYLATE, MENTHOL, CAMPHOR (SYNTHETIC)) SPRAY [VIADERMA DISTRIBUTION, INC] 2 Current NDC, Legacy NDC, 2 package rows 20231209_ab52cd0e-34fa-41c7-9ce7-1183c2aff8d8.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 109 of 152 · 3,029 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 71262-008-55 71262000855 1 BOTTLE in 1 CARTON (71262-008-55) / 55 mL in 1 BOTTLE 1 bottle 2021-06-01 0000-00-00 No No Current