WALGREENS BOIL PAIN RELIEF- boil pain relief ointment

Walgreens Boil Pain Relief by

Drug Labeling and Warnings

Walgreens Boil Pain Relief by is a Otc medication manufactured, distributed, or labeled by Walgreens Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts 

Active Ingredient

Benzocaine 20% 

Purpose 

Pain Reliever 

Uses 

• for the temporary relief of pain and discomfort casued by boils

WarningsFor external use only

Do not use 

• for more than 3 days 

Ask a doctor before use if you have

• boils on the lips,nose ,cheeks or foreehead. 

When using this product 

• avoid contact with eyes 

Stop use and ask a doctor if

• fevers occur
• redness around the bolis develops
• condition worsens or does not improve
• symptoms persist for mroe thna 3 days 
• symptoms clear up and occur again within a few days. 

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of childern. If swallowed, get medical help

or contact poison Control Center (1-800-222-1222) right away. 

Directions 

• Adults and children 2 years and older; Apply to the affected areas not more than 2 times daily
• Children under 2 years;ask a doctor

Other Information 

Store as controlled room temperature 20-25 C ( 68-77F)

Inactive ingredients

Beeswax, Camphor, Eucalyptus Oil, Lanolin, Menthol, Paraffin, Petrolatum, Thymol

Principal display panel 1 oz 

Walgreens          NDC: 0363-9095-28

Boil Pain Relief Ointment 

Benzocaine 20%/ Pain reliever

NET WT 1 OZ (28g)

INGREDIENTS AND APPEARANCE

WALGREENS BOIL PAIN RELIEF 
boil pain relief ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-9095
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	200 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
EUCALYPTUS OIL (UNII: 2R04ONI662)
LANOLIN (UNII: 7EV65EAW6H)
MENTHOL (UNII: L7T10EIP3A)
PARAFFIN (UNII: I9O0E3H2ZE)
PETROLATUM (UNII: 4T6H12BN9U)
THYMOL (UNII: 3J50XA376E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9095-28	1 in 1 CARTON	02/01/2024
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/01/2024

Labeler - Walgreens Company (008965063)