HYDROGEN PEROXIDE liquid

Hydrogen Peroxide by

Drug Labeling and Warnings

Hydrogen Peroxide by is a Otc medication manufactured, distributed, or labeled by UBQ Industries, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Hydrogen Peroxide 3%

Hydrogen Peroxide 3% v/v First aid anitseptic debriding agent

First aid antiseptic debriding agent

First aid antiseptic debriding agent

Indications and usage section

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 occasional sore mouth

Warnings Section

For external use only

Do not use

In the eyes or apply over large areas of the body
Longer than one week

Ask a doctor before use if you have

Deep puncture wounds, animal bites or serious burns

Stop use and ask a doctor if

Swelling, rash, or fever develops
The condition persists or gets worse
Sore mouth symptoms do not improve in 7 days
Irritation, pain, or redness persists or worsens

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions For use as a first aid antiseptic:

Clean affected area
If bandaged, let fry first
Apply small amount of product on affected area 1 – 3 times a day
May be covered with a sterile bandage
For use as an oral debriding agent (oral rinse):
Adults and children 2 years of age
Mix with equal amount of water
Swish around in the mouth over affect area for at least 1 minute and then spit out. Do not swallow
Use up to 4 times daily after meals and at bedtime or as directed by a dentist or doctor
Children under 12 years: should be supervised in the use of this product
Children under 2 years of age: consult a doctor or dentist

Other Information

Keep tightly closed and in a dark place at room temperature
Do not shake bottle. Hold away from face when opening

Inactive Ingredients

Purified water

Package Label - Principal Display Panel

236 ml NDC: 80668-313-04

473.2 ml NDC: 80668-313-03

18927 ml NDC: 80668-313-01

946.4 ml NDC: 80668-313-02

INGREDIENTS AND APPEARANCE

HYDROGEN PEROXIDE 
hydrogen peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80668-313
Route of Administration	DENTAL, ORAL, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	0.03 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80668-313-01	18927 mL in 1 PAIL; Type 0: Not a Combination Product	03/20/2020
2	NDC: 80668-313-02	946.4 mL in 1 JUG; Type 0: Not a Combination Product	03/20/2020
3	NDC: 80668-313-03	473.2 mL in 1 JUG; Type 0: Not a Combination Product	03/20/2020
4	NDC: 80668-313-04	236 mL in 1 JUG; Type 0: Not a Combination Product	03/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/20/2020

Labeler - UBQ Industries, LLC (069021187)

Registrant - UBQ Industries, LLC (069021187)

Establishment
Name	Address	ID/FEI	Business Operations
UBQ Industries, LLC		069021187	manufacture(80668-313) , relabel(80668-313) , repack(80668-313)