Relief

Product NDC
50730-7502
11-digit product format
507307502
Labeler code
50730
Product ID
50730-7502_0bc97563-7db2-40b8-b08c-b55acd9baec4
Type
HUMAN OTC DRUG
Nonproprietary name
witch hazel
Dosage form
SWAB
Route
RECTAL; TOPICAL
Labeler
H and P Industries, Inc. dba Triad Group
Application
part346
Marketing category
OTC MONOGRAPH FINAL
Marketing start
1997-01-14
Marketing end
0000-00-00
Substance
WITCH HAZEL
Active strength
1 mL/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50730-7502-12019-10-21C16284748780-1956f9ecf-dae8-621f-e053-dbdaa90a74adDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50730-7502-1Relief40 in 1 JARSWAB401

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50730-7502RELIEF (WITCH HAZEL) SWAB [H AND P INDUSTRIES, INC. DBA TRIAD GROUP]1Legacy NDC, 1 package rows20091123_58c232b8-0793-4079-baee-22479a8ed3b9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
844379witch hazel 50 % Medicated PadPSN58c232b8-0793-4079-baee-22479a8ed3b91
844379witch hazel 500 MG/ML Medicated PadSCD58c232b8-0793-4079-baee-22479a8ed3b91
844379witch hazel 50 % Medicated PadSY58c232b8-0793-4079-baee-22479a8ed3b91
844379witch hazel 50 % Medicated WipesSY58c232b8-0793-4079-baee-22479a8ed3b91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
50730-7502-15073075020140 in 1 JARHistorical