Salonpas LIDOCAINE PLUS by Hisamitsu America, Inc.
Dosage form: liquid
Ingredients: BENZYL ALCOHOL 10.0000g in 100g, LIDOCAINE HYDROCHLORIDE 4.0000g in 100g
Labeler: Hisamitsu America, Inc.
NDC Code: 55328-901
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.
Benzyl alcohol 10%
Lidocaine HCl 4%
For temporary relief of pain
For external use only
Keep away from fire or flame
Do not use
- on wounds or damaged skin
- in large quantities
- 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
- skin reactions occur, such as rash, itching, redness, irritaion, pain, swelling and blistering
- conditions worsen
- 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.
Adults and children 12 years of age and over:
- clean and dry affected area
- apply to affected area not more than 3 to 4 times daily
Children under 12 years of age:
consult a doctor
- Avoid storing product in direct sunlight
- Protect product from excessive moisture
- Store with lid closed tighly
aloe barbadensis leaf juice, aminomethyl propanol, carbomer, SD alcohol 40-B, water
Questions or comments?
Toll free 1-800-826-8861
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Salonpas LIDOCAINE PLUS Pain Relieving Liquid
4% LIDOCAIN MAXIMUM STRENGTH *
plus 10% Benzyl alcohol
- 2 Powerful Anesthetics
- Fast Acting
- Numbing Relief
MADE IN USA
3 FL OZ (88 mL)
|SALONPAS LIDOCAINE PLUS
benzyl alcohol, lidocaine hydrochloride liquid
|Product Type||HUMAN OTC DRUG||Item Code (Source)||NDC:55328-901
|Route of Administration||TOPICAL, PERCUTANEOUS, TRANSDERMAL||DEA Schedule||
|Active Ingredient/Active Moiety
|Ingredient Name||Basis of Strength||Strength
|BENZYL ALCOHOL (BENZYL ALCOHOL) ||BENZYL ALCOHOL||10.0000 g in 100 g
|LIDOCAINE HYDROCHLORIDE (LIDOCAINE) ||LIDOCAINE HYDROCHLORIDE ANHYDROUS||4.0000 g in 100 g
|ALOE VERA LEAF||
|#||Item Code||Package Description
|1||NDC:55328-901-03||1 TUBE in 1 BOX
|1||80 g in 1 TUBE
|Marketing Category||Application Number or Monograph Citation||Marketing Start Date||Marketing End Date
|OTC monograph not final||part348||09/01/2017||
|Labeler - Hisamitsu America, Inc.
Hisamitsu America, Inc.
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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.