Home NDC 73492-711 Ultra Strength Pain Relief Balm
Product NDC 73492-711
11-digit product format 734920711
Labeler code 73492
Product ID 73492-711_4583ba32-cb31-6fdf-e063-6394a90a6803
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR, MENTHOL
Dosage form OINTMENT
Route TOPICAL
Labeler ALAINA HEALTHCARE PRIVATE LIMITED
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-27
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 110; 110 mg/g; mg/g
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 Ultra Strength Pain Relief Balm
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 110 mg/g MENTHOL 110 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET 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 1089847 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 73492-711-18 Ultra Strength Pain Relief Balm 18 g in 1 BOTTLE, GLASS OINTMENT 18 4 73492-711-18 Ultra Strength Pain Relief Balm 1 in 1 CARTON OINTMENT 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73492-711 ULTRA STRENGTH PAIN RELIEF BALM (CAMPHOR, MENTHOL) OINTMENT [ALAINA HEALTHCARE PRIVATE LIMITED] 3 Current NDC, Legacy NDC, 2 package rows 20241215_80779d1f-0c2a-4ae5-9ed7-eb6877f734ba.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 Marketing start Marketing end Sample Exclude flag Status 73492-711-18 73492071118 1 BOTTLE, GLASS in 1 CARTON (73492-711-18) / 18 g in 1 BOTTLE, GLASS 2022-01-27 0000-00-00 No No Current