Pain Relief Gel Roll On

Product NDC
69396-184
11-digit product format
693960184
Labeler code
69396
Product ID
69396-184_50b1a42e-f7ee-74db-e063-6294a90a7d89
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Trifecta Pharmaceuticals USA
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-04-27
Substance
MENTHOL
Active strength
40 g/L
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pain Relief Gel Roll On
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL40 g/L

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui415974

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69396-184-01Pain Relief Gel Roll On1 in 1 BOXGEL11
69396-184-01Pain Relief Gel Roll On0.074 L in 1 BOTTLEGEL0.0741
69396-184-03Pain Relief Gel Roll On0.074 L in 1 BOTTLEGEL0.0741
69396-184-03Pain Relief Gel Roll On3 in 1 BOXGEL31

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN50b1a420-d5cd-6d61-e063-6294a90a04511
415974menthol 0.04 MG/MG Topical GelSCD50b1a420-d5cd-6d61-e063-6294a90a04511
415974menthol 4 % Topical GelSY50b1a420-d5cd-6d61-e063-6294a90a04511

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69396-184-01693960184011 BOTTLE in 1 BOX (69396-184-01) / .074 L in 1 BOTTLE1 bottle2026-04-30NoNoCurrent
69396-184-03693960184033 BOTTLE in 1 BOX (69396-184-03) / .074 L in 1 BOTTLE3 bottle2026-04-30NoNoCurrent