83632-004 Hemorrhoid and Fissure Relief Ointment

Manufacturer
Zhengzhou Zhuoqing Trading Co., Ltd.
Effective date
2025-03-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:40:53

Label at a glance#

ProductHemorrhoid and Fissure Relief
Active ingredientALPHA-TOCOPHEROL, ALOE, LIDOCAINE, WITCH HAZEL
Label structure12 sections

Indications and uses

1.Helps relieve the pain, itching and bumning associated with hemorrhoids 2.Temporarily reduces the swelling associated with iritated hemorrhoidal tissue and other anorectal disorders 3.Temporarily provides a coating for relief of anorectal discomforts 4.Temporarily protects imitated areas and infamed perianal skin

Dosage and administration

Adults: When practical, cleanse the affected area with mild soap and warm water and ring thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Children under 12 year of age: Consult a doctor.

Storage and handling

●Keep away from direct sunlight or heat. ●Store at room temperature 15C-30°C(59°F-86°F)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Witch Hazel 3%
Lidocaine 4%
Vitamin E 1%
Aloe 1%

OTC - PURPOSE SECTION

Reduces swelling, anti-iflammatory.
Pain relief.
Promotes wound healing.
Moisturizing, repairing, ant-infammatory

Uses

INDICATIONS & USAGE SECTION

1.Helps relieve the pain, itching and bumning associated with hemorrhoids
2.Temporarily reduces the swelling associated with iritated hemorrhoidal tissue and other anorectal disorders
3.Temporarily provides a coating for relief of anorectal discomforts
4.Temporarily protects imitated areas and infamed perianal skin

WARNINGS SECTION

Warnings: For external and intrarectal use only
Ask a doctor or pharmacist before use if you are presently taking a prescription drug.

OTC - DO NOT USE SECTION

DO not use If allergic to any of the ingredients
If pregnant or breast-feeding, ask a health professional before use.

When usina this product

OTC - WHEN USING SECTION

●DO not exceed the recommended daily dosage unless as directed by a doctor.
●Do not use the product with an applicator if the introduction of the applicator
into the rectum Causes additional pain. Consult a doctor promptly.

OTC - STOP USE SECTION

●Condition worsens or does not improve within 7 days
●Bleeding occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, in case of excessive use, get help from a health professional right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults: When practical, cleanse the affected area with mild soap and warm water and ring thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.

Children under 12 year of age: Consult a doctor.

Other Information

STORAGE AND HANDLING SECTION

●Keep away from direct sunlight or heat.
●Store at room temperature 15C-30°C(59°F-86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Moschus Artifactus, Bovis Calculus Artifactus, Margarita, Borneolum syntheticum,
Succinum, Borax, Vaseline, L anolin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

22

33

44

55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83632-004HEMORRHOID AND FISSURE RELIEF (HEMORRHOID AND FISSURE RELIEF OINTMENT) OINTMENT [ZHENGZHOU ZHUOQING TRADING CO., LTD.]2Unmatched20250304_2f6a9d52-30da-207e-e063-6294a90a9344.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83632-00483632-004-01, 83632-004-02, 83632-004-03, 83632-004-04, 83632-004-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
4850ac0f-91c6-6939-e063-6294a90ad71f2f6a9d52-30da-207e-e063-6294a90a93442026-01-13WarningsExact identifier
spl set id: 2f6a9d52-30da-207e-e063-6294a90a9344

Reported adverse events (FAERS/openFDA)#

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