DCH Pain Relieving

Product NDC
72839-031
11-digit product format
728390031
Labeler code
72839
Product ID
72839-031_29a4d0a2-d9a9-c38a-e063-6294a90a1e96
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol 2%
Dosage form
GEL
Route
TOPICAL
Labeler
Derma Care Research Labs, LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-08-12
Substance
MENTHOL
Active strength
2 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
DCH Pain Relieving
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL2 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui311502

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72839-031-08DCH Pain Relieving227 g in 1 BOTTLE, PLASTICGEL2272

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72839-031DCH PAIN RELIEVING (MENTHOL 2%) GEL [DERMA CARE RESEARCH LABS, LLC]2Current NDC, 1 package rows20241222_ff49ee63-6a87-c7a7-e053-6294a90a77a3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311502menthol 2 % Topical GelPSNff49ee63-6a87-c7a7-e053-6294a90a77a32
311502menthol 0.02 MG/MG Topical GelSCDff49ee63-6a87-c7a7-e053-6294a90a77a32
311502menthol 2 % Topical GelSYff49ee63-6a87-c7a7-e053-6294a90a77a32
311502menthol 2 % topical stickSYff49ee63-6a87-c7a7-e053-6294a90a77a32

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72839-031-0872839003108227 g in 1 BOTTLE, PLASTIC (72839-031-08) 227 g2021-08-12NoNoCurrent