Oral Pain Relief

Product NDC
67510-0058
11-digit product format
675100058
Labeler code
67510
Product ID
67510-0058_615afe0d-b55d-8efc-e053-2991aa0ab306
Type
HUMAN OTC DRUG
Nonproprietary name
Oral Pain Reliever
Dosage form
GEL
Route
TOPICAL
Labeler
Kareway Product, Inc.
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-07-17
Marketing end
0000-00-00
Substance
BENZOCAINE
Active strength
200 mg/g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67510-0058-42020-01-31C16284748780-19d75b9cf-ec84-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67510-0058-4Oral Pain Relief1 in 1 CARTONGEL12
67510-0058-4Oral Pain Relief11.9 g in 1 TUBEGEL11.92

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67510-0058ORAL PAIN RELIEF (ORAL PAIN RELIEVER) GEL [KAREWAY PRODUCT, INC.]2Legacy NDC, 2 package rows20171228_b5d833d9-e367-4927-8e4f-790ad41d2502.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
238910benzocaine 20 % Oral GelPSNb5d833d9-e367-4927-8e4f-790ad41d25022
238910benzocaine 0.2 MG/MG Oral GelSCDb5d833d9-e367-4927-8e4f-790ad41d25022
238910benzocaine 20 % (180-220 MG per 1 GM) Oral GelSYb5d833d9-e367-4927-8e4f-790ad41d25022

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
67510-0058-4675100058041 in 1 CARTONHistorical