FDA.reportPublic FDA data

Major Medi-Pads

Manufacturer
Major Pharmaceuticals | PREMIER CARE INDUSTRIES, INC
Effective date
2025-12-05
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:20:25

Label at a glance#

ProductMajor Medi-Pads
Active ingredientWITCH HAZEL
Label structure9 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: Cleanse the area by gently wiping, patting or blotting.  If necessary, repeat until all matter is removed from the area. apply externally to the affected area up to 6 times daily or after each bowel movement. After application, discard pad and wash hands. children under 12 years of age:Consult a doctor Dispose of pad in trash after use. Do not flush

Storage and handling

store at room temperature 15-30°C (59-86°F)

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)

If pregnant or breast-feeding

PREGNANCY SECTION

ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adult: Cleanse the area by gently wiping, patting or blotting.  If necessary, repeat until all matter is removed from the area.
  • apply externally to the affected area up to 6 times daily or after each bowel movement. After application, discard pad and wash hands.
  • children under 12 years of age:Consult a doctor
  • Dispose of pad in trash after use.
  • Do not flush

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature 15-30°C (59-86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Alcohol, Glycerin, Phenoxyethanol, Aloe, Decyl Glucoside, Potassium Sorbate, Propylene Glycol, Sodium Benzoate, Citric Acid

Questions or Comments?

OTC - QUESTIONS SECTION

(800) 616-2471

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0904-6829-60

MAJOR MEDI-PADS

Hemorrhoidal Pads with Witch Hazel

Cools, soothes and helps relieve local discomfort associated with hemorrhoids

Convenient to use

100 pads 3.0 in dia (7.5 cm dia)

Compare to Tucks active ingredient*

* This product is not manufactured or distrbiuted by McNEIL-PPC, Inc., owner of registered trademark Trucks

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
844379witch hazel 50 % Medicated PadPSN5
844379witch hazel 500 MG/ML Medicated PadSCD5
844379witch hazel 50 % Medicated PadSY5
844379witch hazel 50 % Medicated WipesSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0904-6829-60Major Medi-Pads2.9 g in 1 PACKETCLOTH2.95
0904-6829-60Major Medi-Pads100 in 1 PACKAGECLOTH1005

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-6829-60EA - Each0904-6829e85321f2-b647-400b-9f5c-8b0786d29e5212019-05-02

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
0904-68290904-6829-60

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
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALOEV5VD430YW9IACT
DECYL GLUCOSIDEZ17H97EA6YIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM BENZOATEOJ245FE5EUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WITCH HAZEL101I4J0U34ACTIB
WATER059QF0KO0RIACT

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
Major Medi-PadsWITCH HAZELMajor Pharmaceuticalsd2a314a2-98ab-4ac0-9e90-1a8c1303958f2025-12-05WarningsExact identifier
ndc (package): 0904-6829-60
ndc (product): 0904-6829
ndc11 (package): 00904682960
spl id: 4539e5a6-0db0-02e3-e063-6294a90ad7a7
spl set id: d2a314a2-98ab-4ac0-9e90-1a8c1303958f

Reported adverse events (FAERS/openFDA)#

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