Home NDC 82939-000 ORCA Complete Menthol Pain Reliever
Product NDC 82939-000
11-digit product format 829390000
Labeler code 82939
Product ID 82939-000_0c06e3d2-4481-f4b5-e063-6394a90a0608
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL
Dosage form LIQUID
Route ORAL
Labeler ORCA Products, LLC
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-15
Substance MENTHOL, UNSPECIFIED FORM
Active strength 20 mg/mL
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 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 82939-000 82939-000-01 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 ORCA Complete Menthol Pain Reliever
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 20 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 2611702 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 82939-000-01 ORCA Complete Menthol Pain Reliever 10 mL in 1 BOTTLE, GLASS LIQUID 10 3 82939-000-01 ORCA Complete Menthol Pain Reliever 1 in 1 BOX LIQUID 1 3 82939-000-02 ORCA Complete Menthol Pain Reliever 1 in 1 BOX LIQUID 1 3 82939-000-02 ORCA Complete Menthol Pain Reliever 13 mL in 1 BOTTLE LIQUID 13 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82939-000 ORCA COMPLETE MENTHOL PAIN RELIEVER (MENTHOL) LIQUID [ORCA PRODUCTS, LLC] 3 Current NDC, Legacy NDC, 4 package rows 20231209_99990e27-d66b-4d61-97f2-6a76066eb8b8.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 9 of 40 · 786 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 82939-000-01 82939000001 1 BOTTLE, GLASS in 1 BOX (82939-000-01) > 10 mL in 1 BOTTLE, GLASS 2022-09-15 0000-00-00 No No Current 82939-000-02 82939000002 1 BOTTLE in 1 BOX (82939-000-02) / 13 mL in 1 BOTTLE 1 bottle 2023-09-15 No No Current