Home NDC 63299-001 MENTHOL AND METHYL SALICYLATE
Product NDC 63299-001
11-digit product format 632990001
Labeler code 63299
Product ID 63299-001_4344ef98-ce28-2cec-e063-6294a90a1c74
Type HUMAN OTC DRUG
Nonproprietary name ELECTRIC MEDICATED BALM ULTRA STRENGTH
Dosage form OINTMENT
Route TOPICAL
Labeler FEI FAH MEDICAL MANUFACTURING PTE LTD
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-19
Marketing end 2029-11-22
Substance MENTHOL; METHYL SALICYLATE
Active strength 16; 32 g/100g; g/100g
NDC exclude flag No
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 MENTHOL AND METHYL SALICYLATE Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 16 g/100g METHYL SALICYLATE 32 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup LAV5U5022Y Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2002730 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 63299-001-01 MENTHOL AND METHYL SALICYLATE 1 in 1 BOX OINTMENT 1 3 63299-001-01 MENTHOL AND METHYL SALICYLATE 70 g in 1 JAR OINTMENT 70 3 63299-001-02 MENTHOL AND METHYL SALICYLATE 10 g in 1 JAR OINTMENT 10 3 63299-001-02 MENTHOL AND METHYL SALICYLATE 1 in 1 BOX OINTMENT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63299-001 MENTHOL AND METHYL SALICYLATE (ELECTRIC MEDICATED BALM ULTRA STRENGTH) OINTMENT [FEI FAH MEDICAL MANUFACTURING PTE LTD] 2 Current NDC, Legacy NDC, 4 package rows 20241121_91e6d3b9-25bb-4015-9d96-bd27f93e5ada.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 18 of 153 · 3,057 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 63299-001-01 63299000101 1 JAR in 1 BOX (63299-001-01) / 70 g in 1 JAR 1 jar 2024-10-19 2029-11-22 No No Current 63299-001-02 63299000102 1 JAR in 1 BOX (63299-001-02) / 10 g in 1 JAR 1 jar 2024-10-19 2029-11-22 No No Current