SALONPAS DEEP RELIEVING- camphor, menthol, methyl salicylate gel 
Hisamitsu America, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredients

Camphor 3.1%

Menthol 10.0%

Methyl salicylate 15.0%

Purpose

Topical analgesic

Uses

For temporary relief of minor aches and pains of muscles and joints associated with:

Warnings

For external use only

Allergy alert:

If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Flammable:

Keep away from fire or flame.

Do not use

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

When using this product
  • use only as directed
  • avoid contact with the eyes, mucous membranes or rashes
  • do not bandage tightly

Stop use and ask a doctor if
  • conditions worsen
  • skin reactions such are redness, itching, rash, excessive irritation, burning sensation, swelling or blistering occur
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

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

Adults and children 12 years of age and over:

Children under 12 years of age: consult a doctor

Other information

Inactive ingredients

ammonium acryloyldimethyltaurate/VP copolymer, dimethyl isosorbide, propylene glycol, SD alcohol 40-B, water

Questions or comments?

Toll free 1-800-826-8861

www.salonpas.us

Principal Display Panel

Hisamitsu

Non-Greasy Gel

Salonpas DEEP Relieving Gel

TOPICAL ANALGESIC

MADE IN USA

2.75 OZ (78 g)

image of 78g box label

SALONPAS DEEP RELIEVING 
camphor, menthol, methyl salicylate gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55328-900
Route of AdministrationTOPICAL, PERCUTANEOUS, TRANSDERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)3.10 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10.00 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE15.00 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55328-900-021 in 1 BOX06/01/2013
178 g in 1 TUBE; Type 1: Convenience Kit of Co-Package
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/2013
Labeler - Hisamitsu America, Inc. (191877802)

Revised: 11/2018
Document Id: 04dcd8e1-8637-41df-a7fb-b63cc3c9bd9f
Set id: a4ddb2b9-d023-4c8c-9285-93d51f93207d
Version: 3
Effective Time: 20181128
 
Hisamitsu America, Inc.