Label: SALONPAS PAIN RELIEVING JET- menthol, methyl salicylate aerosol, spray
- NDC Code(s): 46581-440-04, 46581-440-99
- Packager: Hisamitsu Pharmaceutical Co., Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated December 17, 2018
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
-
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 where sparks come out
- do not use in a confined space
- do not puncture or incinerate container. Contents under pressure.
- do not expose to temperature exceeding 120 degrees F (48 degrees C)
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
- avoid inhalation
-
Directions
Adults and children 12 years of age and over:
- shake the can very well before use
- to avoid frostbite, hold the can 4 inches (10 cm) away from the skin, and spray each affected area for no longer than 1 second
- apply to affected area not more than 3 to 4 times daily
Children under 12 years of age: consult a docutor
- Other information
- Inactive ingredient
- Questions or comments?
- Principal Display Panel
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
SALONPAS PAIN RELIEVING JET
menthol, methyl salicylate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46581-440 Route of Administration TOPICAL, PERCUTANEOUS, TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 3.0 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 10.0 g in 100 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46581-440-04 14.6 g in 1 CAN; Type 0: Not a Combination Product 05/01/2011 2 NDC:46581-440-99 3.6 g in 1 CAN; Type 0: Not a Combination Product 05/01/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/01/2011 Labeler - Hisamitsu Pharmaceutical Co., Inc. (690539713) Registrant - Hisamitsu Pharmaceutical Co., Inc. (690539713)