HEMORRHOID

Manufacturer
Zhengzhou Zhuoqing Trading Co., Ltd.
Effective date
2023-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:57:11

Label at a glance#

ProductHEMORRHOID
Active ingredientZINC OXIDE, PETROLATUM
Label structure12 sections

Indications and uses

For the temporary relieve of local itching and discomfort associated with hemorrhoids. Temporarily forms a protective coating over inflamed tissues to help prevent drying of tissues. Temporarily protects irritated areas , relieves burning. Provides temporary relief from skin irritations. Temporarily provides a coating for relief of anorectal discomforts. Temporarily protects the inflamed , irritated anorectal surf...

Dosage and administration

Adults : When practical , cleanse the affected area with mild soap and warm water and ring thoroughly . Gently dry by atting 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 15°C-30°C ( 59F-86F )

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Petrolatum 77.99%

Calamine 7.6%

OTC - PURPOSE SECTION

Protectant

Astringent

Temporarily protects inflamed perianal skin.

Temporarily relieves the symptoms of periana skin irritation

Uses

INDICATIONS & USAGE SECTION

For the temporary relieve of local itching and discomfort associated with hemorrhoids.

Temporarily forms a protective coating over inflamed tissues to help prevent drying of tissues.

Temporarily protects irritated areas , relieves burning.

Provides temporary relief from skin irritations.

Temporarily provides a coating for relief of anorectal discomforts.

Temporarily protects the inflamed , irritated anorectal surface to help make bowel movements less painful

WARNINGS SECTION

For external and / or 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.

Do not use the product with an applicator if the introduction of the applicator into the rectum causes additional pain Consult a doctor promptly

When usina this product

OTC - WHEN USING SECTION

Do not exceed the recommended daily dosage unless as directed by a doctor.

Do not use If allergic to any of the ingredients

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

Stop use and ask a doctor if

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 atting 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 15°C-30°C ( 59F-86F )

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Moschus Artifactus , Bovis Calculus Artifactus , Margarita , Borneolum syntheticum , Succinum , Borax , Lanolin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83632-002-0183632-002-0183632-002-0283632-002-0283632-002-0383632-002-0383632-002-0483632-002-0483632-002-0583632-002-0583632-002-0683632-002-0683632-002-0783632-002-0783632-002-0883632-002-08

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2668058petrolatum 77.99 % / zinc oxide 7.6 % Rectal CreamPSN1
2668058petrolatum 780 MG/ML / zinc oxide 76 MG/ML Rectal CreamSCD1
2668058petrolatum 77.99 % / zinc oxide 7.6 % Rectal CreamSY1
2668058petrolatum 780 MG/ML / ZNO 76 MG/ML Rectal CreamSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83632-002-01HEMORRHOID40 g in 1 BOXCREAM401
83632-002-02HEMORRHOID60 g in 1 BOXCREAM601
83632-002-03HEMORRHOID40 g in 1 BOXCREAM401
83632-002-04HEMORRHOID60 g in 1 BOXCREAM601
83632-002-05HEMORRHOID120 g in 1 BOXCREAM1201
83632-002-06HEMORRHOID40 g in 1 BOXCREAM401
83632-002-07HEMORRHOID60 g in 1 BOXCREAM601
83632-002-08HEMORRHOID120 g in 1 BOXCREAM1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83632-002HEMORRHOID CREAM [ZHENGZHOU ZHUOQING TRADING CO., LTD.]18 package rows20231022_0831954e-61c6-a468-e063-6294a90a32f4.zip

Products#

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

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NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
0831954e-61c7-a468-e063-6294a90a32f40831954e-61c6-a468-e063-6294a90a32f42023-10-20WarningsExact identifier
spl id: 0831954e-61c7-a468-e063-6294a90a32f4
spl set id: 0831954e-61c6-a468-e063-6294a90a32f4

Reported adverse events (FAERS/openFDA)#

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