FDA.reportPublic FDA data

Tucks Triple Relief Hemorrhoidal

Manufacturer
Blistex Inc.
Effective date
2024-12-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:51:00

Label at a glance#

ProductTucks Triple Relief Hemorrhoidal
Active ingredientWHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

for the temporary relief of pain, soreness, or burning helps relieve the local itching and discomfort associated with hemorrhoids temporarily shrinks hemorrhoidal tissue temporarily provides a coating for relief of anorectal discomforts temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful temporarily forms a protective coating over inflamed tissues to help preven...

Dosage and administration

Adults: when practical, clean the affected area with mild soap and warm water and rinse thoroughly gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product when first opening the tube, remove foil seal. Do not use if foil seal is broken. apply externally or in the lower portion of the anal canal only apply externally to the affected area up to 4 times daily for applic...

Storage and handling

www.tucks.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientsPurpose
Glycerin 15% (w/w)Protectant
Phenylephrine HCl 0.25% (w/w)Vasoconstrictor
Pramoxine HCl 1.0% (w/w)Local anesthetic
White Petrolatum 16% (w/w)Protectant

Uses

INDICATIONS & USAGE SECTION

  • for the temporary relief of pain, soreness, or burning
  • helps relieve the local itching and discomfort associated with hemorrhoids
  • temporarily shrinks hemorrhoidal tissue
  • temporarily provides a coating for relief of anorectal discomforts
  • temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful
  • temporarily forms a protective coating over inflamed tissues to help prevent drying of tissues
  • may provide a cooling sensation

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

  • do not exceed the recommended daily dosage unless directed to do so by a doctor
  • do not put directly in 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 reactions develop due to ingredients in this product
  • the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults:

  • when practical, clean the affected area with mild soap and warm water and rinse thoroughly
  • gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product
  • when first opening the tube, remove foil seal. Do not use if foil seal is broken.
  • apply externally or in the lower portion of the anal canal only
  • apply externally to the affected area up to 4 times daily
  • for application in the lower anal canal, remove cover from dispensing cap. Attach dispensing cap to tube. Lubricate dispensing cap well, then gently insert dispensing cap partially into the anus.
  • thoroughly clean dispensing cap after each use and replace cover
  • children under 12 years of age: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

arachidyl alcohol, arachidyl glucoside, beeswax, behenyl alcohol, disodium EDTA, ethylhexylglycerin, hamamelis virginiana (witch hazel) water, microcrystalline wax, phenoxyethanol, polyglyceryl-3 diisostearate, polysorbate 60, purified water, sorbitan isostearate, stearyl behenate

PRINCIPAL DISPLAY PANEL - 26 g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW

TUCKS®

TRIPLE RELIEF
HEMORRHOIDAL CREAM

Hemorrhoidal Cream

MAXIMUM STRENGTH
PAIN RELIEF

helps relieve pain
from burning, itching
& discomfort

shrinks swollen
hemorrhoidal tissue

cools & soothes
sensitive areas

BRAND USED
BY HOSPITALS

with
WITCH
HAZEL

Net Wt. 0.9 oz. (26 g) - 1 tube

PRINCIPAL DISPLAY PANEL - 26 g Tube Carton
PRINCIPAL DISPLAY PANEL - 26 g Tube Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2701523glycerin 15 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 16 % Rectal CreamPSN1
2701523glycerin 150 MG/ML / petrolatum 160 MG/ML / phenylephrine hydrochloride 2.5 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal CreamSCD1
2701523glycerin 15 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 16 % Rectal CreamSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e4e263da-1c53-440f-bb80-b7a575843b5aProduct name120260313
d2168cac-a261-415a-9c78-3522859fa720Product name320251124
05a8cdd1-eeb8-409e-b938-0778225eca7dProduct name420250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9Product name820250220
f489e8f3-5c9e-4818-b539-a73587edcfc7Product name220240229
0f7ae452-206d-4fc4-868d-56fc47074084Product name120231011
b5abe2e3-39a1-43eb-9bff-f3c1653fe3dfProduct name220190930
e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814Product name320150910
42f3c020-f1b3-89bc-7bdc-e1f10e680485Product name120140508
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508
e949165d-714d-e548-2b76-0cb5def16f30Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10157-2126-1Tucks Triple Relief Hemorrhoidal26 g in 1 TUBE, WITH APPLICATORCREAM261
10157-2126-1Tucks Triple Relief Hemorrhoidal1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10157-2126TUCKS TRIPLE RELIEF HEMORRHOIDAL (WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE) CREAM [BLISTEX INC.]1Current NDC, 2 package rows20250108_bf892e90-2d9b-4fa0-8ee4-8a2736be6c30.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10157-212610157-2126-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
WHITE PETROLATUMB6E5W8RQJ4ACTIB
GLYCERINPDC6A3C0OXACTIB
PRAMOXINE HYDROCHLORIDE88AYB867L5ACTIB
PHENYLEPHRINE HYDROCHLORIDE04JA59TNSJACTIB
WATER059QF0KO0RIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
POLYSORBATE 60CAL22UVI4MIACT
STEARYL BEHENATEA68S9UI39DIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
HAMAMELIS VIRGINIANA TOP WATERNT00Y05A2VIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
DOCOSANOL9G1OE216XYIACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
YELLOW WAX2ZA36H0S2VIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EDETATE DISODIUM7FLD91C86KIACT

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
Tucks Triple Relief HemorrhoidalWHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDEBlistex Inc.bf892e90-2d9b-4fa0-8ee4-8a2736be6c302024-12-24WarningsExact identifier
ndc (package): 10157-2126-1
ndc (product): 10157-2126
ndc11 (package): 10157212601
spl id: 19acdb94-4437-4eaf-aa16-0bef186d9f8a
spl set id: bf892e90-2d9b-4fa0-8ee4-8a2736be6c30

Reported adverse events (FAERS/openFDA)#

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