GOODSENSE Maximum Strength Medicated

Product NDC
50804-211
11-digit product format
508040211
Labeler code
50804
Product ID
50804-211_453a56d2-cd45-a854-e063-6394a90a969d
Type
HUMAN OTC DRUG
Nonproprietary name
WITCH HAZEL
Dosage form
CLOTH
Route
TOPICAL
Labeler
GEISS, DESTIN & DUNN, INC
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-07-27
Substance
WITCH HAZEL
Active strength
50 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
GOODSENSE Maximum Strength Medicated
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
WITCH HAZEL50 g/100g

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
5453a12b-e775-4101-bd3a-337857e9e167Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-211-48GOODSENSE Maximum Strength Medicated48 in 1 PACKAGECLOTH486
50804-211-48GOODSENSE Maximum Strength Medicated2.9 g in 1 PACKETCLOTH2.96

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50804-211-48EA - Each50804-211119876e7-3e2f-40ef-80d1-9b5e2483c55112022-03-09

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-211GOODSENSE MAXIMUM STRENGTH MEDICATED (WITCH HAZEL) CLOTH [GEISS, DESTIN & DUNN, INC]5Current NDC, Legacy NDC, 2 package rows20241211_5453a12b-e775-4101-bd3a-337857e9e167.zip

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 29 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TrueLipids Relieve and Protect CL MDWHITE PETROLATUMClaridei Laboratories, Inc.27c0af9b-f397-dec3-e063-6394a90aed8b2025-12-15WarningsExact identifier
application number: M016
Truelipids TrueLips Lip Balm CL MDWHITE PETROLATUMClaridei Laboratories, Inc.27c155dc-f194-6750-e063-6394a90a20b12025-12-15WarningsExact identifier
application number: M016
Aquaphor HealingPETROLATUMBeiersdorf Inc0a17bf6f-6114-4647-a509-65999255c37b2025-12-15WarningsExact identifier
application number: M016
Aquaphor OriginalPETROLATUMBeiersdorf Incd38ec874-7b8c-4b9b-92b6-286278bb67f32025-12-15WarningsExact identifier
application number: M016
Aquaphor Healing Diaper RashZINC OXIDEBeiersdorf Incdec07dfc-67a2-46ad-8fab-828488bdba152025-12-15WarningsExact identifier
application number: M016
HealthWise Diabetic Foot CreamDIMETHICONE, PETROLATUMVeridian Healthcare7ba0ac53-c78c-4a70-a977-a082f731919e2025-12-15WarningsExact identifier
application number: M016
Aquaphor Lip Protectant and SunscreenPETROLATUM, AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONEBeiersdorf Inca43c2802-9cf1-477e-9f93-e11cf40b480d2025-12-15WarningsExact identifier
application number: M016
Prequel Barrier Therapy Rich Skin Protectant CreamSKIN PROTECTANT CREAMThe Center Brands, LLC39945806-8f29-020b-e063-6294a90a9fc62025-12-13WarningsExact identifier
application number: M016
ECZEMACOLLOIDAL OATMEALSmith Amish, LLC20c4bc16-ba20-47ec-e063-6394a90a8b4e2025-12-12WarningsExact identifier
application number: M016
Humco CalagesicCALAMINE AND PRAMOXINE HYDROCHLORIDEHumco Holding Group, Inc.8c43590d-56ec-4588-8076-99ba94a166852025-12-11WarningsExact identifier
application number: M016
Soteri Skin Baby Eczema Relief CreamCOLLOIDAL OATMEALSoteri Skin, Inc41d88ff2-22aa-8447-e063-6294a90aea0e2025-12-10WarningsExact identifier
application number: M016
Soteri Skin Active Flare-Up Eczema Relief CreamCOLLOIDAL OATMEALSoteri Skin, Inc.41b558d9-55ba-97ff-e063-6394a90a963b2025-12-10WarningsExact identifier
application number: M016
CeraVe Developed With Dermatologist Baby Eczema Relief CreamOATMEALL'Oreal USA Products Inc5d392529-9f0c-40bc-92ca-7003f8e64b1c2025-12-09WarningsExact identifier
application number: M016
CeraVe Developed with Dermatologists Eczema Relief MoisturizingCOLLOIDAL OATMEALL'Oreal USA Products Incc4dde987-fe4e-4f8e-8f3a-1bc12c9588ed2025-12-09WarningsExact identifier
application number: M016
First Aid Beauty FAB Ultra Repair Intense Hydration Skin ProtectantCOLLOIDAL OATMEALThe Procter & Gamble Manufacturing Company446ddb19-4bdb-6827-e063-6394a90a6af82025-12-09WarningsExact identifier
application number: M016
First Aid Beauty FAB Ultra Repair Intense Hydration Skin Protectant Warm VanillaCOLLOIDAL OATMEALThe Procter & Gamble Manufacturing Company45864832-51bb-4e24-e063-6294a90ab5542025-12-09WarningsExact identifier
application number: M016
AquaSootheAQUASOOTHEDynarex Corporation45878c3c-d05d-984c-e063-6294a90a46612025-12-09WarningsExact identifier
application number: M016
Soteri Skin Long-Term Eczema Relief CreamCOLLOIDAL OATMEALSoteri Skin, Inc41d752cb-3866-e840-e063-6394a90acc372025-12-09WarningsExact identifier
application number: M016
Earths Care EczemaOATMEALDLC Laboratories, Inc.f72e2adf-8930-458f-a6cc-9b240b2f5eba2025-12-08WarningsExact identifier
application number: M016
First Aid Beauty FAB Ultra Repair Skin Protectant Sparkling GrapefruitCOLLOIDAL OATMEALThe Procter & Gamble Manufacturing Company4575ba40-009c-26e0-e063-6394a90adee62025-12-08WarningsExact identifier
application number: M016

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
844379witch hazel 50 % Medicated PadPSN5453a12b-e775-4101-bd3a-337857e9e1676
844379witch hazel 500 MG/ML Medicated PadSCD5453a12b-e775-4101-bd3a-337857e9e1676
844379witch hazel 50 % Medicated PadSY5453a12b-e775-4101-bd3a-337857e9e1676
844379witch hazel 50 % Medicated WipesSY5453a12b-e775-4101-bd3a-337857e9e1676

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50804-211-485080402114848 PACKET in 1 PACKAGE (50804-211-48) / 2.9 g in 1 PACKET48 packet2017-07-270000-00-00NoNoCurrent