WALGREENS PAIN RELIEF WITH LIDOCAINE- lidocaine, phenylephrine hcl spray

Walgreens Pain Relief with Lidocaine by

Drug Labeling and Warnings

Walgreens Pain Relief with Lidocaine by is a Otc medication manufactured, distributed, or labeled by Walgreens Co, Derma Care Research Labs, Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 5%, Phenylephrine HCl 0.25%

PURPOSE

Hemorrhoidal (Anorectal)

INDICATIONS & USAGE

Helps relieve the local itching and discomfort associated with anorectal disorders or inflammation.

WARNINGS

For external use only.

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

When using this product avoid contact with eyes, do not exceed recommended 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 rectal 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.

PREGNANCY OR BREAST FEEDING

Ask a professional before use.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

When practical, cleanse the affected area with mild soap and warm water, rinse thoroughly and gently pat dry, spray affected area, wash hands after applying. Adults and children 12 years and older: apply externally to the affected area up to 4 times a day. Children under 12 years of age: consult a doctor.

INACTIVE INGREDIENT

Alcohol denat., aloe barbadensis leaf extract, citric acid, disodium EDTA, glycerin, malic acid, menthol, propyl gallate, propylene glycol, sodium benzoate, water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS PAIN RELIEF WITH LIDOCAINE 
lidocaine, phenylephrine hcl spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 g  in 100 g
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	0.25 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
MENTHOL (UNII: L7T10EIP3A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID (UNII: 2968PHW8QP)
MALIC ACID (UNII: 817L1N4CKP)
PROPYL GALLATE (UNII: 8D4SNN7V92)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1026-03	107.7 g in 1 CAN; Type 0: Not a Combination Product	03/24/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	03/24/2026

Labeler - Walgreens Co (008965063)

Registrant - Derma Care Research Labs (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(0363-1026)