76986-032 NERANTE Hemorrhoid Cream

Manufacturer
Guangdong Quadrant Ecological Technology Co., Ltd.
Effective date
2026-09-14
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-09-17 01:00:47

Label at a glance#

ProductNERANTE Hemorrhoid Cream
Active ingredientLIDOCAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 5%

OTC - PURPOSE SECTION

Local Anesthetic

INDICATIONS & USAGE SECTION


For the temporary relief of local and anorectal itching and discomfort associated with anorectal disorders.
For the burning and soreness.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken or irritated skin.

OTC - WHEN USING SECTION


Use only as much as recommended, unless a doctor advises otherwise.
Do not insert into the rectum with fingers or any mechanical device or applicator.

OTC - STOP USE SECTION


An allergic reaction is observed.
Symptoms such as redness, irritation, swelling, pain, orothers begin or worsen.
Does not show improvement within 7 days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION


For adults and children 12 years and older: When practical, clean the area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth beforeapplying.
Apply up to 6 times daily.
Children under 12 years: Ask a doctor.

INACTIVE INGREDIENT SECTION

CETYL ALCOHOL
STEARYL ALCOHOL
GLYCERIN
MINERAL OIL
SODIUM POLYACRYLOYLDIMETHYL TAURATE
HYDROGENATED POLYDECENE
TRIDECETH-10
WATER
PROPYLENE GLYCOL
CETEARETH-25
STEARIC ACID
GLYCERYL STEARATE
DIMETHICONE
BENZYL ALCOHOL
PHENOXYETHANOL
BENZOIC ACID
ARNICA MONTANA FLOWER EXTRACT
TOCOPHERYL ACETATE
TRIETHANOLAMINE
EUCALYPTUS GLOBULUS LEAF OIL
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
LECITHIN
CARBOMER
EMU OIL
XANTHAN GUM
POTASSIUM LAURYL PHOSPHATE
DIPOTASSIUM PHOSPHATE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel
label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76986-03276986-032-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-08-21daily-update2026-08-25 01:01:54
12026-03-23full-release2026-06-01 01:51:07

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
598b7336-64a9-9a3d-e063-6294a90a9ea04dacd4f1-24d8-37ab-e063-6294a90a944d2026-08-21WarningsExact identifier
spl set id: 4dacd4f1-24d8-37ab-e063-6294a90a944d

Reported adverse events (FAERS/openFDA)#

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