BOOBOO BUBBLES- hydrogen peroxide solution

Booboo Bubbles by

Drug Labeling and Warnings

Booboo Bubbles by is a Otc medication manufactured, distributed, or labeled by 72 Seasons LLC, Pharma Nobis LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Hydrogen Peroxide 3%

Purpose

Antiseptic

Indications

As an antiseptic to help prevent infection in minor cuts, scrapes, burns.

As an oral rinse for temporary use in cleaning minor wounds or irritation/inflammation to the mouth and gums resulting from minor dental procedures, orthodontic appliances or accidental injury.

Warnings

For external use except when used as an oral rinse

Do not use

Do not use in the eyes

Do not apply over large areas of the body

Do not use longer than 1 weeks unless directed by a dentist or doctor

Ask a doctor before use if you have

Deep or puncture wounds

Animal bites

Serious burns

Sop use and consult a dentist or doctor if

condition persists or gets worse

sore mouth symptoms do not improve in 7 days

irritation, pain, redness or fever develop

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or contact a Poison Control Cernter immediately.

Directions

For antiseptic use Clean the affected area. Apply a small amount on the area 1 to 3 times daily.

For oral rinse use Adults and children 2 years and older: Mix with an equal amount of water and swish around and over the affected area, then spit out. Use up to 4 times daily or as directed by a dentist or doctor. Children under 2 years of age: Consult a doctor.

Other Information

Keep tightly closed and at controlled room temperature 15 o-30 oC (59 o-86 oF). Do not shake.

Inactive Ingredient

Purified water

Front Panel Label

INGREDIENTS AND APPEARANCE

BOOBOO BUBBLES 
hydrogen peroxide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85324-001
Route of Administration	BUCCAL, TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85324-001-01	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/15/2025

Labeler - 72 Seasons LLC (113832998)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis LLC		118564114	manufacture(85324-001)