Home NDC 70039-300 Professional Therapy MuscleCare Pain Relieving
Product NDC 70039-300
11-digit product format 700390300
Labeler code 70039
Product ID 70039-300_2c670151-ca6c-8d49-e063-6394a90af091
Type HUMAN OTC DRUG
Nonproprietary name Menthol, Camphor
Dosage form OINTMENT
Route CUTANEOUS; TOPICAL
Labeler Active and Innovative Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-01-01
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Active strength 40; 40 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 70039-300-02 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 70039-300-02 0efc9e666f02…f202fb6c5f17…
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
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 40 mg/g CAMPHOR (SYNTHETIC) 40 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 900390 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 70039-300-02 Professional Therapy MuscleCare Pain Relieving 115 g in 1 TUBE OINTMENT 115 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70039-300 PROFESSIONAL THERAPY MUSCLECARE PAIN RELIEVING (MENTHOL, CAMPHOR) OINTMENT [ACTIVE AND INNOVATIVE INC.] 3 Current NDC, Legacy NDC, 1 package rows 20250125_42f1abeb-f6d7-01c3-e054-00144ff88e88.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 48 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 Marketing end Sample Exclude flag Status 70039-300-02 70039030002 115 g in 1 TUBE (70039-300-02) 115 g 2017-01-01 0000-00-00 No No Current 70039-300-40 70039030040 906 g in 1 TUBE (70039-300-40) 906 g 2026-03-16 No No Current