Home NDC 82503-101-11 THE GOO
Product NDC 82503-101
Requested package NDC 82503-101-11
11-digit product format 825030101
Labeler code 82503
Product ID 82503-101_4914f51b-96e4-989e-e063-6394a90a424f
Type HUMAN OTC DRUG
Nonproprietary name METHYL SALICYLATE, MENTHOL, CAMPHOR
Dosage form GEL
Route TOPICAL
Labeler APSM PERFORMANCE, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-04-30
Substance METHYL SALICYLATE; MENTHOL, UNSPECIFIED FORM; CAMPHOR OIL
Active strength 30; 10; 4 g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 THE GOO
Brand name suffix MEDICATED PAIN RELIEF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHYL SALICYLATE 30 g/100mL MENTHOL, UNSPECIFIED FORM 10 g/100mL CAMPHOR OIL 4 g/100mL
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 75IZZ8Y727 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1116730 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 82503-101-11 THE GOOMEDICATED PAIN RELIEF 100 mL in 1 BOTTLE GEL 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82503-101 THE GOO MEDICATED PAIN RELIEF (METHYL SALICYLATE, MENTHOL, CAMPHOR) GEL [APSM PERFORMANCE, LLC] 2 Current NDC, Legacy NDC, 1 package rows 20240120_db4c321c-8cdc-5a11-e053-2995a90a91a1.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 82503-101-11 82503010111 100 mL in 1 BOTTLE (82503-101-11) 100 ml 2022-04-30 0000-00-00 No No Current