FDA.reportPublic FDA data

GOODSENSE Maximum Strength Medicated

Manufacturer
GEISS, DESTIN & DUNN, INC | PREMIER CARE INDUSTRIES, INC
Effective date
2025-12-05
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:20:18

Label at a glance#

ProductGOODSENSE Maximum Strength Medicated
Active ingredientWITCH HAZEL
Label structure8 sections

Indications and uses

helps relieve the local itching and discomfort associated with hemorrhoids temporary relief of irritation and burning. aids in protecting irritated anorectal areas.

Dosage and administration

adult: unfold wipe and cleanse the area by gently wiping, patting or blotting.  If necessary, repeat until all matter is removed from the area. use up to 6 times daily or after each bowel movement and before applying hemorrhoidal treatments, and then discard children under 12 years of age:Consult a doctor Dispose of wipe in trash. do not flush

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Witch hazel 50%

Purpose

OTC - PURPOSE SECTION

Astringent

Uses

INDICATIONS & USAGE SECTION

  • helps relieve the local itching and discomfort associated with hemorrhoids
  • temporary relief of irritation and burning.
  • aids in protecting irritated anorectal areas.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • do not exceed the recommended daily dosage unless directed by a doctor
  • do not put this product into the rectum by using fingers or any mechanical device or applicator.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • bleeding occurs
  • condition worsens or does not improve within 7 days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

  • adult: unfold wipe and cleanse the area by gently wiping, patting or blotting.  If necessary, repeat until all matter is removed from the area.
  • use up to 6 times daily or after each bowel movement and before applying hemorrhoidal treatments, and then discard
  • children under 12 years of age:Consult a doctor
  • Dispose of wipe in trash.
  • do not flush

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature 20-25°C (68-77°F)
  • for vaginal care - cleanse the area by gently wiping, patting, or blotting.  Repeat as needed.
  • for use as moist compress - if necessary, first cleanse the area as previously described. Fold wipe to desire size and place in contact with tissue for a soothing and cooling effect. Leave in place for 15 minutes and repeat as needed.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Aloe, citric acid, Decyl Glucoside, Glycerin, Phenoxyethanol, Potassium Sorbate, Propylene Glycol, Sodium Benzoate, Water.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 50804-211-48

GOODSENSE Maximum Strength

Medicated Wipes with Aloe

Hemorrhoidal Wipes with Witch Hazel

  • Mild everyday wipes
  • Cools, Soothes and Cofmorts
  • Convenient, Easy to use, Flushable Wipes

Compare to active ingredients of PREPARATION H Medicated Wipes

100% satisfaction Guaranteed

48 Wipes

6 X 5 in. (15.2 X12.7 cm)

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
844379witch hazel 50 % Medicated PadPSN6
844379witch hazel 500 MG/ML Medicated PadSCD6
844379witch hazel 50 % Medicated PadSY6
844379witch hazel 50 % Medicated WipesSY6

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50804-21150804-211-48

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ALOEV5VD430YW9IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM BENZOATEOJ245FE5EUIACT
WATER059QF0KO0RIACT
WITCH HAZEL101I4J0U34ACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GOODSENSE Maximum Strength MedicatedWITCH HAZELGEISS, DESTIN & DUNN, INC5453a12b-e775-4101-bd3a-337857e9e1672025-12-05WarningsExact identifier
ndc (package): 50804-211-48
ndc (product): 50804-211
ndc11 (package): 50804021148
spl id: 453a56d2-cd45-a854-e063-6394a90a969d
spl set id: 5453a12b-e775-4101-bd3a-337857e9e167

Reported adverse events (FAERS/openFDA)#

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