ARTHRITIS PAIN RELIEF

Product NDC
83041-101
11-digit product format
830410101
Labeler code
83041
Product ID
83041-101_ece6bea2-19b6-b233-e053-2995a90ad832
Type
HUMAN OTC DRUG
Nonproprietary name
HISTAMINE DIHYDROCHLORIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
PainX LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-11-07
Marketing end
0000-00-00
Substance
HISTAMINE DIHYDROCHLORIDE
Active strength
0 g/100g
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
83041-101-142024-01-30C16284748780-11030e365-0ea7-111a-e063-dadaa90a10e2PAINX - ARTHRITIS PAIN RELIEF (83041-101)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83041-101-14ARTHRITIS PAIN RELIEF119 g in 1 JARCREAM1191

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83041-101ARTHRITIS PAIN RELIEF (HISTAMINE DIHYDROCHLORIDE) CREAM [PAINX LLC]1Legacy NDC, 1 package rows20221108_ece6bea2-19b5-b233-e053-2995a90ad832.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2167855histamine dihydrochloride 0.03 % Topical CreamPSNece6bea2-19b5-b233-e053-2995a90ad8321
2167855histamine dihydrochloride 0.3 MG/ML Topical CreamSCDece6bea2-19b5-b233-e053-2995a90ad8321
2167855histamine dihydrochloride 0.03 % Topical CreamSYece6bea2-19b5-b233-e053-2995a90ad8321

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
83041-101-1483041010114119 g in 1 JAR (83041-101-14) 119 g2022-11-070000-00-00NoNoCurrent