Pain Relief

Product NDC
84638-8201
11-digit product format
846388201
Labeler code
84638
Product ID
84638-8201_1f44466f-0450-70fe-e063-6294a90ad575
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
AEROSOL, SPRAY
Route
TOPICAL
Labeler
Pain Relieving Spray Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-03-31
Substance
MENTHOL
Active strength
70 mg/L
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
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL70 mg/L

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui1086713

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84638-8201-1Pain Relief0.059 L in 1 BOTTLE, SPRAYAEROSOL, SPRAY0.0591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84638-8201PAIN RELIEF (MENTHOL) AEROSOL, SPRAY [PAIN RELIEVING SPRAY INC.]1Current NDC, 1 package rows20250331_1f44466f-044f-70fe-e063-6294a90ad575.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1086713menthol 7 % Topical SprayPSN1f44466f-044f-70fe-e063-6294a90ad5751
1086713menthol 70 MG/ML Topical SpraySCD1f44466f-044f-70fe-e063-6294a90ad5751
1086713menthol 7 % Topical SpraySY1f44466f-044f-70fe-e063-6294a90ad5751

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
84638-8201-184638820101.059 L in 1 BOTTLE, SPRAY (84638-8201-1) 2025-03-31NoNoCurrent