Label: ADVIL TARGETED RELIEF- camphor, capsaicin, menthol, methyl salicylate cream
- NDC Code(s): 0573-6555-45, 0573-6555-48, 0573-6555-51, 0573-6555-54
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 8, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purposes
- Uses
-
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
- Directions
- Other information
- Inactive ingredients
-
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
-
INGREDIENTS AND APPEARANCE
ADVIL TARGETED RELIEF
camphor, capsaicin, menthol, methyl salicylate creamProduct 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)