Ice Blue Pain Alleviating Rub

Product NDC
82988-101
11-digit product format
829880101
Labeler code
82988
Product ID
82988-101_c8b1a1f6-4e27-4e37-b0cd-6171939fd038
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)
Dosage form
GEL
Route
TOPICAL
Labeler
Lemisol Corporation
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-08-31
Marketing end
0000-00-00
Substance
CAMPHOR (NATURAL); MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active strength
0 g/g; g/g; g/g
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82988-101-082024-01-30C16284748780-11030e365-58b4-111a-e063-dadaa90a10e20238f4aa-6f40-489a-9a09-a6ba2d8080b5
82988-101-162024-01-30C16284748780-11030e365-58b4-111a-e063-dadaa90a10e20238f4aa-6f40-489a-9a09-a6ba2d8080b5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82988-101ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) GEL ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) SPRAY [LEMISOL CORPORATION]1Legacy NDC20221221_0238f4aa-6f40-489a-9a09-a6ba2d8080b5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82988-101-0882988010108226.7 g in 1 JAR (82988-101-08) 226.7 g2022-08-310000-00-00NoNoCurrent
82988-101-1682988010116453.5 g in 1 JAR (82988-101-16) 453.5 g2022-08-310000-00-00NoNoCurrent