83632-003 Hemorrhoid and Fissure Relief Ointment

Manufacturer
Zhengzhou Zhuoqing Trading Co., Ltd.
Effective date
2025-02-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:56:10

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 Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83632-003-01Hemorrhoid and Fissure Relief10 g in 1 TUBEPASTE101
83632-003-02Hemorrhoid and Fissure Relief20 g in 1 TUBEPASTE201
83632-003-03Hemorrhoid and Fissure Relief28 g in 1 TUBEPASTE281
83632-003-04Hemorrhoid and Fissure Relief42.5 g in 1 TUBEPASTE42.51
83632-003-05Hemorrhoid and Fissure Relief57 g in 1 TUBEPASTE571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83632-003HEMORRHOID AND FISSURE RELIEF (HEMORRHOID AND FISSURE RELIEF OINTMENT) PASTE [ZHENGZHOU ZHUOQING TRADING CO., LTD.]15 package rows20250228_2f081d29-7411-f41f-e063-6294a90a282a.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
83632-00383632-003-01, 83632-003-02, 83632-003-03, 83632-003-04, 83632-003-05

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
2f082d53-ab46-7ba5-e063-6394a90a26682f081d29-7411-f41f-e063-6294a90a282a2025-02-26WarningsExact identifier
spl id: 2f082d53-ab46-7ba5-e063-6394a90a2668
spl set id: 2f081d29-7411-f41f-e063-6294a90a282a

Reported adverse events (FAERS/openFDA)#

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