Walgreens Lidocaine Spray

Manufacturer
Walgreens Co | Derma Care Research Labs, LLC
Effective date
2023-11-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:18:25

Label at a glance#

ProductLidocaine Hemorrhoid
Active ingredientWITCH HAZEL, PHENYLEPHRINE HYDROCHLORIDE, LIDOCAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 5%, Phenylephrine HCl 0.25%, Witch Hazel 50%

OTC - PURPOSE SECTION

Anorectal; anesthetic, vasoconstrictor, astringent

INDICATIONS & USAGE SECTION

  • Temporarily shrinks hemorrhoidal tissue
  • Temporarily reduces the swelling and irritation associated with hemorrhoids and other anorectal disorders
  • aids in protecting irritated anorectal areas

INDICATIONS & USAGE SECTION

Temporarily shrinks hemorrhoidal tissue. Temporarily reduces the swelling and irritation associated with hemorrhoids and other anorectal disorders. Aids in protecting irritated anorectal areas.

WARNINGS SECTION

For external use only.

Flammable. Do not use while smoking or near heat or flame.

When using this product

  • keep away from children
  • avoid spraying in eyes
  • contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F
  • do not exceed the 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
  • certain persons can develop allergic reactions to ingredients in this product. If the symptoms being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor.

Ask a doctor or pharmacist before use if you have

  • heart disease, high blood pressure, thyroid disease, diabetes, difficulty in urination due to enlargement of the prostate gland
  • are presently taking a prescription drug for high blood pressure or depression

Stop use and ask a doctor if

  • bleeding occurs
  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • needed for longer than 1 week

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222).

DOSAGE & ADMINISTRATION SECTION

  • Adults: when practical, cleanse the affected are with an appropriate cleansing wipe.
  • Spray rectal area until thoroughly moist. Wipe off excess with tissue.
  • Gently dry by patting or blotting with a tissue or a soft cloth.
  • Apply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement.
  • Children under 12 years of age, consult a doctor.

INACTIVE INGREDIENT SECTION

alcohol, aloe barbadensis leaf extract, anthemis nobilis flower extract, benzophenone-4, benzyl alcohol, centella asiatica extract,disodium EDTA, epilobium angustifolium extract, ethylhexylglycerin, glycerin, hydroxyethylcellulose, polysorbte 40, propylene glycol, sodium citrate, tocopherol, tocopheryl acetate, water.

OTC - QUESTIONS SECTION

1-800-925-4733

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-15670363-1567-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
10a7742a-613d-92ae-e063-6394a90a740905b76342-598d-fab8-e063-6394a90aa9392024-02-05WarningsExact identifier
spl set id: 05b76342-598d-fab8-e063-6394a90aa939

Reported adverse events (FAERS/openFDA)#

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