Home NDC 72342-050 Pain Relieving Liniment
Product NDC 72342-050
11-digit product format 723420050
Labeler code 72342
Product ID 72342-050_142d99a3-82d9-758a-e063-6294a90ab7f5
Type HUMAN OTC DRUG
Nonproprietary name Camphor (Natural) and Menthol, Unspecified Form
Dosage form SPRAY
Route TOPICAL
Labeler J.R. Watkins, LLC.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-09-01
Substance CAMPHOR (NATURAL); MENTHOL, UNSPECIFIED FORM
Active strength 3.5; 2.5 g/100mL; g/100mL
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 Pain Relieving Liniment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (NATURAL) 3.5 g/100mL MENTHOL, UNSPECIFIED FORM 2.5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination N20HL7Q941 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2198969 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72342-050-19 Pain Relieving Liniment 118 mL in 1 BOTTLE, SPRAY SPRAY 118 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72342-050 PAIN RELIEVING LINIMENT (CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM) SPRAY [J.R. WATKINS, LLC.] 4 Current NDC, Legacy NDC, 1 package rows 20240403_97a0c839-0927-4e54-aee2-ded2016ac4a0.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 48 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 72342-050-18 72342005018 1 BOTTLE, SPRAY in 1 BOX (72342-050-18) > 118 mL in 1 BOTTLE, SPRAY 2019-09-01 0000-00-00 No No Current 72342-050-19 72342005019 118 mL in 1 BOTTLE, SPRAY (72342-050-19) 118 ml 2019-09-01 No No Current