Pain Be Gone

Product NDC
82721-001
11-digit product format
827210001
Labeler code
82721
Product ID
82721-001_2ce15484-38f2-014d-e063-6294a90aced2
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
CREAM
Route
TOPICAL
Labeler
Back to Earth Inc.
Application
M014
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-07-27
Substance
MENTHOL
Active strength
9.6 mg/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 Be Gone
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL9.6 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82721-001-01Pain Be Gone50 mL in 1 TUBECREAM503
82721-001-02Pain Be Gone120 mL in 1 TUBECREAM1203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82721-001PAIN BE GONE (MENTHOL) CREAM [BACK TO EARTH INC.]3Current NDC, 2 package rows20250130_f49e718b-ef89-b648-e053-2a95a90a96c8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82721-001-018272100010150 mL in 1 TUBE (82721-001-01) 50 ml2023-07-27NoNoCurrent
82721-001-0282721000102120 mL in 1 TUBE (82721-001-02) 120 ml2023-07-27NoNoCurrent