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NDC 00363-0871-99 Hydrogen Peroxide 30 mg/mL Details

Hydrogen Peroxide 30 mg/mL

Hydrogen Peroxide is a TOPICAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreens Co.. The primary component is HYDROGEN PEROXIDE.

Product Information

NDC	00363-0871
Product ID	0363-0871_9e29ff09-4bbe-4f85-b7b8-252ed2003d8e
Associated GPIs	92000020002010
GCN Sequence Number	009801
GCN Sequence Number Description	hydrogen peroxide SOLUTION 3 % MISCELL
HIC3	W8D
HIC3 Description	OXIDIZING AGENTS
GCN	45121
HICL Sequence Number	004267
HICL Sequence Number Description	HYDROGEN PEROXIDE
Brand/Generic	Generic
Proprietary Name	Hydrogen Peroxide
Proprietary Name Suffix	n/a
Non-Proprietary Name	HYDROGEN PEROXIDE
Product Type	HUMAN OTC DRUG
Dosage Form	SOLUTION
Route	TOPICAL
Active Ingredient Strength	30
Active Ingredient Units	mg/mL
Substance Name	HYDROGEN PEROXIDE
Labeler Name	Walgreens Co.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00363-0871-99 (00363087199)

Pricing Information	N/A
NDC Package Code	0363-0871-99
Billing NDC	00363087199
Package	237 mL in 1 BOTTLE, SPRAY (0363-0871-99)
Marketing Start Date	1996-03-27
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL eea239fe-554f-4487-9312-3ab0af27d530 Details

Active ingredient

Hydrogen peroxide (stabilized) 3%

Purpose

First Aid Antiseptic

Oral Debriding Agent

Uses

first aid to help prevent the risk of infection in minor cuts, scrapes and burns
aids in the removal of phlegm, mucus, or other secretions associated with occcasional sore mouth

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 have

deep or puncture wounds, animal bites or serious burns

Stop use and ask a doctor if

if condition persists or gets worse
sore mouth symptoms do not improve in 7 days
irritation, pain, 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 affected area 1 to 3 times a day
may be covered with a sterile bandage
if bandaged, let dry first

Oral debriding agent:

adults, children over 2 years of age:
mix with an equal amount of water
swish around in the mouth over the affected area for at least 1 minute, then spit out
use up to 4 times daily after meals and at bedtime
children under 12 years of age should be supervised in the use
children under 2 years of age: consult a dentist, doctor

Other information

keep tightly closed and at controlled room temperature. Do not shake bottle. Hold away from face when opening.

inactive ingredient

purified water

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED walgreens.com

MADE IN U.S.A. WITH U.S. AND FOREIGN COMPONENTS

Questions or comments? 1-888-593-0593

principal display panel

Well at Walgreens

WALGREENS PHARMACIST RECOMMENDED

Hydrogen Peroxide 3% Topical Solution USP

First Aid antiseptic

Oral Debriding Agent

Use as a gargle or rinse
For treatment of minor cuts & abrasions

DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING

24 FL OZ (710 mL)

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE

hydrogen peroxide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-0871
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	30 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0363-0871-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/1996
2	NDC:0363-0871-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/1996
3	NDC:0363-0871-50	710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/1996
4	NDC:0363-0871-99	237 mL in 1 BOTTLE, SPRAY; Type 1: Convenience Kit of Co-Package	03/27/1996

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/27/1996

Labeler - Walgreens Co. (008965063)

Registrant - Vi Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi Jon, LLC		790752542	manufacture(0363-0871)

Revised: 5/2022

Document Id: 9e29ff09-4bbe-4f85-b7b8-252ed2003d8e

Set id: eea239fe-554f-4487-9312-3ab0af27d530

Version: 12

Effective Time: 20220506