BABYO2- colloidal silver and glycerin solution

BabyO2 by

Drug Labeling and Warnings

BabyO2 by is a Otc medication manufactured, distributed, or labeled by Oxigenesis, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients                                                          Purpose

Colloidal Silver 2 mg ................................................   Skin Protectant

Glycerin (Plant) 2 mg................................................   Skin Protectant

PURPOSE

Uses

Relieves and prevents the discomfort and symptoms from: diaper rash, chaffed skin, minor burns and abrasions.

WARNINGS

Warnings

For external use only.

Do not use over puncture wounds, infections or lacerations.

Avoid contact with the eyes.

ASK DOCTOR

WHEN USING

STOP USE

Stop use and ask a doctor if condition worsens or does not improve in 7 days.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INDICATIONS & USAGE

Directions

Change wet and solid diapers promptly. Cleanse diaper area and dry. Apply ointment liberally as often necessary with every diaper change, especially at bedtime.

STORAGE AND HANDLING

Other information

Sstore at 20°-25°C (68° -70° F)

INACTIVE INGREDIENT

Inactive ingredients

Distilled water, Sodium Chloride, Hydroxypropyl Starch Phosphate.

DOSAGE & ADMINISTRATION

Marketed & Distributed by:

Oxigenesis, Inc.
2917 Union Road, Suite B
Paso Robles, CA 93446 USA
805-549-0275

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BABYO2 
colloidal silver and glycerin solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72136-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	2 mg  in 240 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	2 mg  in 240 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE NA-22 (UNII: VMP9781061)
HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT) (UNII: 9M44R3409A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72136-005-01	240 mL in 1 TUBE; Type 0: Not a Combination Product	02/26/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/26/2019

Labeler - Oxigenesis, Inc. (006774725)

Registrant - Oxigenesis, Inc. (006774725)

Establishment
Name	Address	ID/FEI	Business Operations
Oxigenesis, Inc.		006774725	manufacture(72136-005)