Pain Relief Gel-Tube

Product NDC
84008-003
11-digit product format
840080003
Labeler code
84008
Product ID
84008-003_42c9380a-3630-9175-e063-6294a90a5db9
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
Bullet point LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-11-03
Substance
MENTHOL
Active strength
.04 g/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pain Relief Gel-Tube
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL.04 g/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui415974

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84008-003-01Pain Relief Gel-Tube73 mL in 1 BOTTLEGEL731
84008-003-02Pain Relief Gel-Tube1 in 1 BOXGEL11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN42c93789-9758-54b7-e063-6394a90ac3981
415974menthol 0.04 MG/MG Topical GelSCD42c93789-9758-54b7-e063-6394a90ac3981
415974menthol 4 % Topical GelSY42c93789-9758-54b7-e063-6394a90ac3981

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84008-003-018400800030173 mL in 1 BOTTLE73 mlHistorical
84008-003-02840080003021 BOTTLE in 1 BOX (84008-003-02) / 73 mL in 1 BOTTLE (84008-003-01) 1 bottle2025-11-03NoNoHistorical