Walgreen Co. Pain Relief Cream Drug Facts

Manufacturer
Walgreen Company
Effective date
2021-11-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:29:08

Label at a glance#

Productpain relief
Active ingredientGLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, PETROLATUM
Label structure9 sections

Indications and uses

• for temporary relief of pain, soreness and 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

Dosage and administration

• adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before applying cream. • when first opening the tube, puncture foil seal with top end of cap • apply externally or in the lower portion of the anal canal only • apply externally to the affected area up to 4 times daily, especially at night, i...

Storage and handling

• store at 20°-25°C (68°-77°F)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Glycerin 14.4%

Phenylephrine HCl 0.25%

Pramoxine HCl 1%

White petrolatum 15%

Purpose

OTC - PURPOSE SECTION

Protectant

Vasoconstrictor

Local anesthetic

Uses

INDICATIONS & USAGE SECTION

  1. for temporary relief of pain, soreness and burning
  2. helps relieve the local itching and discomfort associated with hemorrhoids
  3. temporarily shrinks hemorrhoidal tissue
  4. temporarily provides a coating for relief of anorectal discomforts
  5. temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

Warnings

WARNINGS SECTION

For external use only

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  1. heart disease
  2. high blood pressure
  3. thyroid disease
  4. diabetes
  5. trouble urinating due to an enlarged 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

  1. do not exceed the recommended daily dosage unless directed by a doctor
  2. do not put into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

OTC - STOP USE SECTION

  1. bleeding occurs
  2. condition worsens or does not improve within 7 days
  3. an allergic reaction develops
  4. the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional 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

  1. adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before applying cream.
  2. when first opening the tube, puncture foil seal with top end of cap
  3. apply externally or in the lower portion of the anal canal only
  4. apply externally to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement
  5. 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 partway into the anus.
  6. thoroughly cleanse dispensing cap after each use and replace cover
  7. children under 12 years of age: ask a doctor

Other information

STORAGE AND HANDLING SECTION

  1. store at 20°-25°C (68°-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf extract, butylated hydroxyanisole, carboxymethylcellulose sodium, cetyl alcohol, citric acid, edetate disodium, glyceryl monostearate, laureth-23, methylparaben, mineral oil, panthenol, propyl gallate, propylparaben, purified water, sodium benzoate, steareth-2, steareth-20, stearyl alcohol, vitamin E, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

1-800-719-9260

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VALUE SIZE

HEMORRHOIDAL

Pain Relief Cream

Compare to Preparation H® Cream active ingredients

MAXIMUM STRENGTH

+ ALOE & VITAMIN E

CREAM

Rapid, soothing relief from painful burning, itching & discomfort

Shrinks swollen hemorrhoidal tissue ● Protects irritated tissue

NET WT 1.8 OZ (51 g)

pain-relief-cream-image
pain-relief-cream-image

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-5019-24GM - Gram0363-50195af66202-7e8b-4e72-895a-f4601b64afdb12022-06-06

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-50190363-5019-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
7deb2223-ce98-499d-8bc8-5409803ba5987fec7b38-ddf5-4d84-902d-e42c0d01102b2021-11-05WarningsExact identifier
spl id: 7deb2223-ce98-499d-8bc8-5409803ba598
spl set id: 7fec7b38-ddf5-4d84-902d-e42c0d01102b

Reported adverse events (FAERS/openFDA)#

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