BT Pain Relief

Product NDC
82198-0012
11-digit product format
821980012
Labeler code
82198
Product ID
82198-0012_0aa61368-2851-7dba-e063-6394a90af0ee
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, METHYL SALICYLATE
Dosage form
SPRAY
Route
TOPICAL
Labeler
Big 5 Nutrition LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-01-01
Substance
MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active strength
100; 50 mg/mL; 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
BT Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM100 mg/mL
METHYL SALICYLATE50 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A, LAV5U5022Y
Rxcui1875611

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82198-0012-1BT Pain Relief70 mL in 1 BOTTLESPRAY701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82198-0012BT PAIN RELIEF (MENTHOL, METHYL SALICYLATE) SPRAY [BIG 5 NUTRITION LLC]1Current NDC, 1 package rows20240101_91324910-27cf-424f-9e9b-6173f2d7acbf.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1875611menthol 10 % / methyl salicylate 5 % Topical SprayPSN91324910-27cf-424f-9e9b-6173f2d7acbf1
1875611menthol 100 MG/ML / methyl salicylate 50 MG/ML Topical SpraySCD91324910-27cf-424f-9e9b-6173f2d7acbf1
1875611menthol 10 % / methyl salicylate 5 % Topical SpraySY91324910-27cf-424f-9e9b-6173f2d7acbf1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82198-0012-18219800120170 mL in 1 BOTTLE (82198-0012-1) 70 ml2024-01-01NoNoCurrent