Home NDC 70039-201 Professional Therapy MuscleCare
Product NDC 70039-201
11-digit product format 700390201
Labeler code 70039
Product ID 70039-201_42f1e14a-3ac7-01c1-e054-00144ff8d46c
Type HUMAN OTC DRUG
Nonproprietary name Menthol, Camphor
Dosage form GEL
Route CUTANEOUS; TOPICAL
Labeler Active and Innovative Inc.
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-01-01
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 100; 140 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Professional Therapy MuscleCare
Brand name suffix Turbo
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 140 mg/g CAMPHOR (SYNTHETIC) 100 mg/g
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 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1923001 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 70039-201-03 Professional Therapy MuscleCareTurbo 85 g in 1 BOTTLE, WITH APPLICATOR GEL 85 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70039-201 PROFESSIONAL THERAPY MUSCLECARE TURBO (MENTHOL, CAMPHOR) GEL [ACTIVE AND INNOVATIVE INC.] 1 Current NDC, Legacy NDC, 1 package rows 20170517_42f1e14a-3ac6-01c1-e054-00144ff8d46c.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 1 of 1 · 1 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 70039-201-03 70039020103 85 g in 1 BOTTLE, WITH APPLICATOR (70039-201-03) 85 g 2017-01-01 0000-00-00 No No Current