ORAL B MOUTH SORE SPECIAL CARE RINSE- sodium fluoride rinse 
The Procter & Gamble Manufacturing Company

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Oral-B Mouth Sore Special Care Rinse

Drug Facts

Active ingredient

Hydrogen Peroxide 1.5%

Purpose

oral debriding/wound cleansing

Uses

Warnings

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

Directions

• adults and children 6 yrs. & older:

Rinse with 20 mL

Swish around in the mouth over the affected area for at least 1 minute and then spit out.

Use up to four times daily after meals and at bedtime or as directed by a dentist or doctor.

do not swallow

supervise use

do not use

Inactive ingredients

citric acid, flavor, glycerin, poloxamer 407, propylene glycol, sodium citrate, sodium hexametaphosphate, sodium saccharin, sucralose, water

Questions?

1-800-862-7442

DISTR. BY ORAL-B, A DIVISION

OF PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 475 mL Bottle Label

Oral-B

HYDROGEN PEROXIDE ORAL DEBRIDING AGENT

MOUTH SORE

SPECIAL CARE ORAL RINSE

For Mouth Sores Including:

SOOTHING MINT

475 mL (16 FL OZ)

962

ORAL B MOUTH SORE  SPECIAL CARE RINSE
sodium fluoride rinse
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-962
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE0.03 mL  in 20 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-962-16475 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/02/2020
2NDC:37000-962-08237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/02/2020
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 07ec67e8-a3ed-a416-e063-6294a90a881e
Set id: a2b5032a-e142-48ae-e053-2995a90ade74
Version: 4
Effective Time: 20231017
 
The Procter & Gamble Manufacturing Company