Label: SALONPAS PAIN RELIEVING LIDOCAINE 4% FLEX- lidocaine patch
- NDC Code(s): 46581-840-07
- Packager: Hisamitsu Pharmaceutical Co., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 17, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
Do not use
- more than 1 patch at a time
- on wounds or damaged skin
- with a heating pad
- if you are allergic to any igredients of this product
When using this product
- use only as directed
- avoid contact with the eyes, mucous membranes or rashes
- do not bandage tightly
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Directions
Adults and children 12 years of age and over:
- clean and dry affected area
- peel film from patch and apply to the skin (see illustration)
- apply 1 patch at a time to affected area, not more than 3 to 4 times daily
- remove patch from the skin after at most 8-hour application
Children under 12 years of age: consult a doctor
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
OTC topical analgesics in patch category
WORLD’S BRAND NO.1
Hisamitsu
NDC#46581-840-07
for temporary relief of pain
PATCH CONTOURS TO YOUR BODY
Adheres as you move, bend, twist, or flex
Salonpas Pain Relieving FLEX Patch LIDOCAINE 4%
APPLY FOR UP TO 8 HOURS
MAXIMUM OTC STRENGTH
• Stretchable
• Thin Fabric
• Strong Adhesion
7 PATCHES
2 3/4" X 3 15/16" (7cm X 10cm)
MADE IN JAPAN -
INGREDIENTS AND APPEARANCE
SALONPAS PAIN RELIEVING LIDOCAINE 4% FLEX
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46581-840 Route of Administration TOPICAL, PERCUTANEOUS, TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 42 mg Inactive Ingredients Ingredient Name Strength ALUMINUM SILICATE (UNII: T1FAD4SS2M) MINERAL OIL (UNII: T5L8T28FGP) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46581-840-07 7 in 1 BOX 03/01/2022 1 1 in 1 POUCH; 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 03/01/2022 Labeler - Hisamitsu Pharmaceutical Co., Inc. (690539713)