ADVIL TARGETED RELIEF- camphor, capsaicin, menthol, methyl salicylate cream

Advil Targeted Relief by

Drug Labeling and Warnings

Advil Targeted Relief by is a Otc medication manufactured, distributed, or labeled by Haleon US Holdings LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Camphor 3.1%

Capsaicin 0.025%

Menthol 10%

Methyl salicylate 15%

Purposes

Topical analgesic

Topical analgesic

Topical analgesic

Topical analgesic

Uses

• Temporarily relieves minor aches and pains of muscles and joints associated with:

• arthritis
• strains
• simple backache
• bruises
• sprains

Warnings

For external use only

• avoid contact with eyes. If eye contact occurs, rinse thoroughly with water.

Do not use

• on wounds or damaged skin
• with a heating pad
• if you are allergic to any ingredients in this product

Ask a doctor before use if you have

• redness over the affected area

When using this product

• do not bandage tightly

Stop use and ask a doctor if

• condition worsens or if symptoms last for more than 7 days
• symptoms clear up and occur again within a few days
• rash, itching or skin irritation develops

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

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• use only as directed
• adults and children 12 years and older: apply to affected area not more than 3 to 4 times daily
• children under 12 years of age: consult your doctor
• wash hands after applying

Other information

• store between 20-25°C (68-77°F)

Inactive ingredients

carbomer homopolymer, cetyl alcohol, cetyl esters wax, emulsifying wax, oleth-3-phosphate, purified water, sodium hydroxide, stearic acid

Questions or comments?

call toll-free 1-800-88-ADVIL

Additional information

DEEP PENETRATING RELIEF

BACK & BODY ACHES

ARTHRITIS & JOINT PAIN

SPRAINS & STRAINS

SORE MUSCLES

STARTS WORKING ON CONTACT

FOR UP TO 8 HOURS OF POWERFUL RELIEF

UP TO 8 HRS

HOW TO USE

Clean and dry affected area

Remove cap

Gently squeeze to dispense cream

Massage cream into skin

Starts to soothe on contact

Do Not Use if tube seal under cap is broken or missing.

Distributed by: Haleon, Warren, NJ 07059

©2023 Haleon group of companies or its licensor.

Trademarks are owned by or licensed to the Haleon group of companies.

For most recent product information, visit www.Advil.com

Made in Canada

PRINCIPAL DISPLAY PANEL

NEW HALEON
DOES NOT CONTAIN THE SAME ACTIVE INGREDIENT AS ADVIL
Advil

TARGETED

RELIEF

PAIN RELIEVING CREAM

4 POWERFUL PAIN FIGHTING INGREDIENTS

Arthritis & Joint Pain

Sprains & Strains

Back & Body aches

Sore Muscles

FOR EXTERNAL USE ONLY

NET WT. 65 g (2.3 oz)

206239 Front

INGREDIENTS AND APPEARANCE

ADVIL TARGETED RELIEF 
camphor, capsaicin, menthol, methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0573-6555
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	31 mg  in 1 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.25 mg  in 1 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	100 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	150 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
CETYL ALCOHOL (UNII: 936JST6JCN)
CETYL ESTERS WAX (UNII: D072FFP9GU)
ISOCETYL STEARATE (UNII: 3RJ7186O9W)
CARNAUBA WAX (UNII: R12CBM0EIZ)
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0573-6555-54	1 in 1 CARTON	03/06/2024
1		65 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 0573-6555-45	1 in 1 CARTON	03/06/2024
2		71 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
3	NDC: 0573-6555-48	3 g in 1 POUCH; Type 0: Not a Combination Product	03/06/2024
4	NDC: 0573-6555-51	1 in 1 CARTON	03/06/2024
4		113.4 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	03/06/2024

Labeler - Haleon US Holdings LLC (079944263)