Home NDC 24909-042 terrasil Bruise and Pain Relief Maximum Strength
Product NDC 24909-042
11-digit product format 249090042
Labeler code 24909
Product ID 24909-042_240b231d-a8b3-c64c-e063-6394a90a7440
Type HUMAN OTC DRUG
Nonproprietary name Camphor, Menthol
Dosage form OINTMENT
Route TOPICAL
Labeler Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-21
Substance MENTHOL; CAMPHOR (NATURAL)
Active strength 16; 11 g/100g; g/100g
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 terrasil Bruise and Pain Relief Maximum Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 16 g/100g CAMPHOR (NATURAL) 11 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 N20HL7Q941 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1802734 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 24909-042-50 terrasil Bruise and Pain Relief Maximum Strength 50 g in 1 TUBE OINTMENT 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24909-042 TERRASIL BRUISE AND PAIN RELIEF MAXIMUM STRENGTH (CAMPHOR, MENTHOL) OINTMENT [AIDANCE SCIENTIFIC, INC., DBA AIDANCE SKINCARE & TOPICAL SOLUTIONS] 1 Current NDC, 1 package rows 20241022_240b231d-a8b2-c64c-e063-6394a90a7440.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 8 of 156 · 3,115 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 24909-042-50 24909004250 50 g in 1 TUBE (24909-042-50) 50 g 2024-10-21 No No Current