Home NDC 70039-302 Professional Therapy MuscleCare Pro
Product NDC 70039-302
11-digit product format 700390302
Labeler code 70039
Product ID 70039-302_1794c494-425d-3eee-e063-6394a90aa08d
Type HUMAN OTC DRUG
Nonproprietary name Camphor, Menthol
Dosage form GEL
Route TOPICAL
Labeler ACTIVE AND INNOVATIVE, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-03
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 4; 10 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 Professional Therapy MuscleCare Pro
Brand name suffix Pain Relieving Cold Gel
Listing expiration 2026-12-31 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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70039-302-16 Professional Therapy MuscleCare ProPain Relieving Cold Gel 453 g in 1 BOTTLE, PUMP GEL 453 5 70039-302-32 Professional Therapy MuscleCare ProPain Relieving Cold Gel 906 g in 1 BOTTLE, PUMP GEL 906 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70039-302 PROFESSIONAL THERAPY MUSCLECARE PRO PAIN RELIEVING COLD GEL (CAMPHOR, MENTHOL) GEL [ACTIVE AND INNOVATIVE, LLC] 5 Current NDC, 2 package rows 20240504_1794c512-5f42-4ec3-e063-6394a90a87cd.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 Sample Exclude flag Status 70039-302-16 70039030216 453 g in 1 BOTTLE, PUMP (70039-302-16) 453 g 2024-05-03 No No Current 70039-302-32 70039030232 906 g in 1 BOTTLE, PUMP (70039-302-32) 906 g 2024-05-03 No No Current