PEROX-A-MINT SOLUTION- hydrogen peroxide mouthwash

Perox-A-Mint Solution by

Drug Labeling and Warnings

Perox-A-Mint Solution by is a Otc medication manufactured, distributed, or labeled by Sage Products, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrogen Peroxide 1.5%

Purpose

Oral Debriding Agent

Use

Aids in the removal of secretions associated with sore mouth

Warnings

Do not use:

• For more than 7 days unless told to do so by a doctor.
• Avoid swallowing.

Stop use and ask a doctor if:

• Sore mouth symptoms do not improve in 7 days.
• Swelling, rash or fever develops.
• Irritation, pain or redness persists of worsens.

Keep out of reach of children.  If more than used for debriding is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Use up to 4 times daily or as directed by a dentist or doctor.
• Adults and children 3 years and over: rinse mouth for approx. one minute with 1/2 Tbsp. Instruct to expectorate.
• Children under 12 years of age:  supervise use.
• Children under 3 years of age:  consult a dentist or doctor.

Inactive Ingredients

Water, menthol flavor, polysorbate 80, phosphoric acid, sodium saccharin, Blue 1 (CI42090), Yellow 6 (CI15985)

QUESTIONS

Questions? Call toll free 800-323-2220

Perox-A-Mint Solution

INGREDIENTS AND APPEARANCE

PEROX-A-MINT SOLUTION 
hydrogen peroxide mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53462-075
Route of Administration	BUCCAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	15 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHOSPHORIC ACID (UNII: E4GA8884NN)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53462-075-30	44 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/21/1998
2	NDC: 53462-075-40	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/21/1998	04/09/2018
3	NDC: 53462-075-60	7 mL in 1 PACKET; Type 0: Not a Combination Product	05/21/1998

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	05/21/1998

Labeler - Sage Products, LLC (054326178)

Registrant - Sage Products, LLC (054326178)