FDA.reportPublic FDA data

medicated pads

Product NDC
11673-614
11-digit product format
116730614
Labeler code
11673
Product ID
11673-614_412203ce-d7fc-28ee-e063-6394a90a929f
Type
HUMAN OTC DRUG
Nonproprietary name
Witch Hazel
Dosage form
PATCH
Route
TOPICAL
Labeler
TARGET CORPORATION
Application
M015
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-05-15
Substance
WITCH HAZEL
Active strength
50 mg/100mg
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage11673-614-10fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage11673-614-1086f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage11673-614-10bd6a592717d7…303034d00443…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
medicated pads
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
WITCH HAZEL50 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
101I4J0U34Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
844379Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
acd0d99d-2a77-4227-bebb-c819f4a52666Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-614-102022-01-28C16284748780-1d6a99b39-334d-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-614-10medicated pads100 in 1 BOXPATCH1006
11673-614-10medicated pads50 mg in 1 PATCHPATCH506

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 18 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hemorrhoid Pain ReliefLIDOCAINETelebrands Corp04164425-ca3b-ef24-e063-6294a90a59d82024-11-20WarningsExact identifier
application number: M015
Hempvana Maximum Strength Pain Relief Topical AnestheticLIDOCAINETelebrands Corpf525075a-d7ee-dad0-e053-2a95a90a6f3f2024-11-20WarningsExact identifier
application number: M015
Curist Lidocaine Numbing ReliefLIDOCAINELittle Pharma, Inc.bff3c422-a0df-6196-e053-2a95a90af0332024-11-20WarningsExact identifier
application number: M015
Hempvana Maximum Strength Pain Relief Topical Anesthetic PlatinumLIDOCAINE 5%Telebrands Corp2774ec41-7366-ac8c-e063-6394a90a1ee22024-11-20WarningsExact identifier
application number: M015
Walgreens Anorectal Lidocaine Cream5% LIDOCAINEWalgreens Company3052fac7-fd68-43f4-9950-8c07288a6b6d2024-11-20WarningsExact identifier
application number: M015
Lidocaine AnorectalLIDOCAINEPatrin Pharma, Inc456d41fe-8449-4980-9291-d7a3b65a900d2024-11-13WarningsExact identifier
application number: M015
MyDermPENYLEPHRINE HCI, WITCH HAZEL, LIDOCAINE HCL,Inspec Solution LLC.2618eba1-9308-a666-e063-6394a90ac3d22024-11-04WarningsExact identifier
application number: M015
Granulotion MedicatedMENTHOL, ZINC OXIDEGL HEALTH, INC.01701780-b160-415b-b34d-3622371794752024-10-29WarningsExact identifier
application number: M015
rexall hemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLDolgencorp Inc0415c51b-5a12-49d4-8968-0131ddb855452024-10-23WarningsExact identifier
application number: M015
Exchange Select HemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLArmy & Air Force Exchange Service8155ed74-9412-498f-998c-4a29c46e934f2024-10-23WarningsExact identifier
application number: M015
Leader HemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLCardinal Health 110, LLC. dba Leaderc4814524-0f4c-4351-a431-5b4b6431fd282024-10-23WarningsExact identifier
application number: M015
basic care hemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLAmazon.com Services LLC617d9213-31f0-4c71-be0c-7961b96e51432024-10-23WarningsExact identifier
application number: M015
Signature Care HemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLSafewaye74b71a1-915d-4e5b-b548-d5cce7945dbd2024-10-23WarningsExact identifier
application number: M015
Equaline HemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLUnited Natural Foods, Inc. dba UNFId29b7824-ff9e-4875-b3de-92721c8add0e2024-10-23WarningsExact identifier
application number: M015
hemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLPublix Super Markets Inca241cb37-7007-4fd8-a12e-f3fc6d6f780e2024-10-22WarningsExact identifier
application number: M015
hemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLKroger Companyd44ca22a-dc20-454d-99aa-403a8c7a3e002024-10-22WarningsExact identifier
application number: M015
rugby hemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLRugby Laboratoriesc1a126b5-0d34-437f-a7ef-8d5cbeb7b03b2024-10-22WarningsExact identifier
application number: M015
hemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLMeijer Distribution Inc1431397e-3515-4794-a494-70667948e14c2024-10-18WarningsExact identifier
application number: M015
signature care hemorrhoidalMINERAL OIL, PETROLATUM, PHENYLEPHRINE HCLSafewayafcf68cf-f187-44d3-ad91-b1e79b182bc62024-10-17WarningsExact identifier
application number: M015
hemorrhoidalCOCOA BUTTER, PHENYLEPHRINE HCLH E B1435432d-5ff2-468b-808d-fb0c99a0717b2024-10-17WarningsExact identifier
application number: M015

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
844379witch hazel 50 % Medicated PadPSNacd0d99d-2a77-4227-bebb-c819f4a526666
844379witch hazel 500 MG/ML Medicated PadSCDacd0d99d-2a77-4227-bebb-c819f4a526666
844379witch hazel 50 % Medicated PadSYacd0d99d-2a77-4227-bebb-c819f4a526666
844379witch hazel 50 % Medicated WipesSYacd0d99d-2a77-4227-bebb-c819f4a526666

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-614-1011673061410100 PATCH in 1 BOX (11673-614-10) / 50 mg in 1 PATCH100 patch2020-05-150000-00-00NoNoCurrent