Medicated Pad

Product NDC
50730-7549
11-digit product format
507307549
Labeler code
50730
Product ID
50730-7549_b0f0c2af-ef39-47ea-b3b4-af08a5c095e8
Type
HUMAN OTC DRUG
Nonproprietary name
witch hazel
Dosage form
SOLUTION
Route
RECTAL; TOPICAL
Labeler
H and P Industries, Inc. dba Triad Group
Application
part346
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2007-02-01
Marketing end
0000-00-00
Substance
WITCH HAZEL
Active strength
1 mL/mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50730-7549-12019-10-21C16284748780-1956f9ecf-d41c-621f-e053-dbdaa90a74adDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50730-7549-1Medicated Pad100 in 1 JARSOLUTION1001
50730-7549-1Medicated Pad2.5 mL in 1 APPLICATORSOLUTION2.51

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50730-7549MEDICATED PAD (WITCH HAZEL) SOLUTION [H AND P INDUSTRIES, INC. DBA TRIAD GROUP]1Legacy NDC, 2 package rows20091208_e3c255d9-9378-4768-8423-472cefd7782d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
844379witch hazel 50 % Medicated PadPSNe3c255d9-9378-4768-8423-472cefd7782d1
844379witch hazel 500 MG/ML Medicated PadSCDe3c255d9-9378-4768-8423-472cefd7782d1
844379witch hazel 50 % Medicated PadSYe3c255d9-9378-4768-8423-472cefd7782d1
844379witch hazel 50 % Medicated WipesSYe3c255d9-9378-4768-8423-472cefd7782d1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
50730-7549-150730754901100 in 1 JARHistorical