AVCOO Pain Relief

Product NDC
84992-003
11-digit product format
849920003
Labeler code
84992
Product ID
84992-003_2e795d36-79ac-1df3-e063-6394a90acade
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
GEL
Route
TOPICAL
Labeler
ADP Health Limited
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-02-18
Substance
MENTHOL
Active strength
4 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL4 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui415974

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84992-003-01AVCOO Pain Relief89 mL in 1 TUBEGEL891
84992-003-02AVCOO Pain Relief89 mL in 1 TUBEGEL891
84992-003-02AVCOO Pain Relief2 in 1 CASEGEL21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84992-003AVCOO PAIN RELIEF (MENTHOL) GEL [ADP HEALTH LIMITED]1Current NDC, 3 package rows20250221_700ce2cf-749e-40be-91c3-850d9b2168ca.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN700ce2cf-749e-40be-91c3-850d9b2168ca1
415974menthol 0.04 MG/MG Topical GelSCD700ce2cf-749e-40be-91c3-850d9b2168ca1
415974menthol 4 % Topical GelSY700ce2cf-749e-40be-91c3-850d9b2168ca1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84992-003-018499200030189 mL in 1 TUBE (84992-003-01) 89 ml2025-02-18NoNoHistorical
84992-003-02849920003022 TUBE in 1 CASE (84992-003-02) / 89 mL in 1 TUBE2 tube2025-02-18NoNoHistorical