HYDROGEN PEROXIDE- hydrogen peroxide solution 
NDC, Inc.

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Hydrogen Peroxide 3%

Drug Facts

Active Ingredient

Hydrogen Peroxide (stabilized) 3%

Purpose

First Aid Antiseptic/Oral Debriding Agent

Uses

Warnings

For external use only

Do not use

  • in the eyes or apply over large areas of the body
  • longer than 1 week

Ask a doctor before use if you havedeep or puncture wounds, animal bites or serious burns.

Stop use and ask a doctor if

  • the condition persists or gets worse
  • sore mouth symptoms do not improve in 7 days
  • irritation, pain, or redness persists or worsens
  • swelling, rash, or fever develops

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

First Aid Antiseptic
  • clean the affected area
  • apply a small amount of product on the area 1 to 3 times a day
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Oral Debriding Agent (oral rinse):

Adults and children 2 years of age & over:

  • mix with an equal amount of water
  • swish around in the mouth over the affected area for at least 1 minute and then spit out
  • use up to 4 times daily after meals and at bedtime or as directed by a dentist or doctor

Other Information

Inactive Ingredient

Purified Water

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

REF: P903016
NDC 43128-001-16

Hydrogen
Peroxide
3% USP

Tamper evident cap for your protection. If ring-band is
detached from cap or missing do not use.

16oz. ( 473mL )

Made in USA for:
NDC, Inc., 407 New Sanford Rd.
La Vergne, TN 37086
www.ProAdvantagebyNDC.com

Pro
ADVANTAGE
®
by NDC

Principal Display Panel

HYDROGEN PEROXIDE 
hydrogen peroxide solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43128-001-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
2NDC:43128-001-08237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00306/01/2014
Labeler - NDC, Inc. (009831413)

Revised: 11/2023
Document Id: 09449a7e-ca10-2c43-e063-6294a90ab21f
Set id: 23f7a9dc-5a6b-4f17-bf76-3864c4881525
Version: 10
Effective Time: 20231103
 
NDC, Inc.