RRHOID RAGE Hemorrhoidal Ointment

Manufacturer
POPPY COLLECTIVE LLC
Effective date
2024-01-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:08:29

Label at a glance#

ProductRRHOID RAGE Hemorrhoidal
Active ingredientLIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE
Label structure7 sections

Indications and uses

–Helps relieve the pain, itching, and burning associated with hemorrhoids. –Temporarily reduces the swelling associated with irritated hemorrhoidal tissue and other anorectal disorders. –Temporarily provides a coating for relief of anorectal discomforts. –Temporarily protects irritated areas and inflamed perianal skin.

Dosage and administration

–When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or soft cloth before applying. –Adults and children 12 years and older: apply externally to the affected area up to 4 times daily. –Children under 12 years of age: consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Phenylephrine HCL 0.25%

Purpose

OTC - PURPOSE SECTION

Local Anesthetic

Vasoconstrictor

Uses

INDICATIONS & USAGE SECTION

–Helps relieve the pain, itching, and burning associated with hemorrhoids.

–Temporarily reduces the swelling associated with irritated hemorrhoidal tissue and other anorectal disorders.

–Temporarily provides a coating for relief of anorectal discomforts.

–Temporarily protects irritated areas and inflamed perianal skin.

Warnings

WARNINGS SECTION

For external use only.

Ask a doctor before use if you have:

OTC - ASK DOCTOR SECTION

–Heart disease; high blood pressure; thyroid disease; diabetes.

–Difficulty in urination due to enlargement of the prostate gland.

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

presently taking a prescription drug for high blood pressure or depression.

When using this product

OTC - WHEN USING SECTION

–Avoid contact with eyes.

–Do not exceed 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.

–Allergic reaction occurs to ingredients in this product.

–Symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase.

If pregnant or breastfeeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a doctor before use.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

–When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or soft cloth before applying.

–Adults and children 12 years and older: apply externally to the affected area up to 4 times daily.

–Children under 12 years of age: consult a doctor.

Other information

SPL UNCLASSIFIED SECTION

–Store at 20-25°C (68-77°F). Excursions permitted to 15-30°C (59-86°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe extract AQ, balsam fir, butylated hydroxyanisol, glycerin, lanolin alcohols, lanolin USP, magnesium sulfate, methyl paraben, mineral oil, petrolatum, propylparaben, witch hazel, white bees wax.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2673304lidocaine 4 % / phenylephrine HCl 0.25 % Rectal OintmentPSN1
2673304lidocaine 0.04 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal OintmentSCD1
2673304lidocaine 4 % / phenylephrine HCl 0.25 % Rectal OintmentSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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e949165d-714d-e548-2b76-0cb5def16f30Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82433-446-00RRHOID RAGE Hemorrhoidal1 in 1 BOXOINTMENT11
82433-446-00RRHOID RAGE Hemorrhoidal28 g in 1 TUBEOINTMENT281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82433-446RRHOID RAGE HEMORRHOIDAL (LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE) OINTMENT [POPPY COLLECTIVE LLC]1Current NDC, 2 package rows20240212_a02a6398-0acd-4aa7-8320-ac586ff12eb3.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
82433-44682433-446-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
RRHOID RAGE HemorrhoidalLIDOCAINE, PHENYLEPHRINE HYDROCHLORIDEPOPPY COLLECTIVE LLCa02a6398-0acd-4aa7-8320-ac586ff12eb32024-01-31WarningsExact identifier
ndc (package): 82433-446-00
ndc (product): 82433-446
ndc11 (package): 82433044600
spl id: 103c47fa-17f7-6e9b-e063-6294a90adce8
spl set id: a02a6398-0acd-4aa7-8320-ac586ff12eb3

Reported adverse events (FAERS/openFDA)#

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