Menthol Pain Relieving Gel

Product NDC
13709-357
11-digit product format
137090357
Labeler code
13709
Product ID
13709-357_513a206c-bbf7-3e51-e063-6294a90adf7a
Type
HUMAN OTC DRUG
Nonproprietary name
Pain Relieving Gel
Dosage form
GEL
Route
TOPICAL
Labeler
NeilMed Pharmaceuticals Inc
Application
M014
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-05-07
Substance
MENTHOL
Active strength
4.54 g/227g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Menthol Pain Relieving Gel
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL4.54 g/227g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui311502

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13709-357-01Menthol Pain Relieving Gel1 in 1 CARTONGEL11
13709-357-01Menthol Pain Relieving Gel227 g in 1 TUBEGEL2271

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311502menthol 2 % Topical GelPSN513a206c-bbf6-3e51-e063-6294a90adf7a1
311502menthol 0.02 MG/MG Topical GelSCD513a206c-bbf6-3e51-e063-6294a90adf7a1
311502menthol 2 % Topical GelSY513a206c-bbf6-3e51-e063-6294a90adf7a1
311502menthol 2 % topical stickSY513a206c-bbf6-3e51-e063-6294a90adf7a1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
13709-357-01137090357011 TUBE in 1 CARTON (13709-357-01) / 227 g in 1 TUBE1 tube2026-05-07NoNoCurrent