Home NDC 70039-285 Professional Therapy MuscleCare Pain Relieving Cold Gel
Product NDC 70039-285
11-digit product format 700390285
Labeler code 70039
Product ID 70039-285_572792bb-281a-36c3-e063-6394a90aa504
Type HUMAN OTC DRUG
Nonproprietary name Camphor, Menthol
Dosage form GEL
Route CUTANEOUS; TOPICAL
Labeler Active and Innovative
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-16
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 4; 10 g/100g; g/100g
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 Professional Therapy MuscleCare Pain Relieving Cold Gel
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 4 g/100g MENTHOL 10 g/100g
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 1039731 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70039-285-40 70039028540 906 g in 1 TUBE (70039-285-40) 906 g 2026-03-16 No No Current