PLAGENTRA BABY BUBBLE WASH- allantoin aerosol, foam

PLAGENTRA BABY BUBBLE WASH by

Drug Labeling and Warnings

PLAGENTRA BABY BUBBLE WASH by is a Otc medication manufactured, distributed, or labeled by C.A Pharm Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Allantoin 0.5%

INACTIVE INGREDIENT

Inactive Ingredients:
Water, Potassium Laureth Phosphate, Cocamidopropyl Betaine, Disodium Cocoamphodiacetate, Glycerin, Polyglutamic Acid, Leuconostoc/Radish Root Ferment Filtrate, Butylene Glycol, Phaseolus Radiatus Extract, Betula Platyphylla Japonica Bark Extract, Rumex Crispus Root Extract, Camellia Sinensis Leaf Extract, Betaine, Sodium Benzoate, Citric Acid, Disodium EDTA, Fragrance

PURPOSE

Purpose: Skin Portectant

WARNINGS

Warnings:
1. Stop using the product and go to a doctor immediately if one of the following symptoms occurs. If immediate care is not sought, the symptoms may worsen :
1) Itching, redness, swelling, rash, etc. 2) If one of the symptoms above occurs due to direct sunlight.
2. Do not apply the product to wounds or skin with dermatitis such as eczema.
3. Storage and Handling, 1) Keep the lid closed after use. 2) Keep the product out of children's reach. 3) Keep away from direct sunlight, do not store at high or low temperature.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of babies and children.

INDICATIONS & USAGE

Indication and usage:
1) Tighten the lid after using it.
2) Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight.
3) Use it in the morning or evening in the bath.

DOSAGE & ADMINISTRATION

Dosage and administration:
Take appropriate amount and gently apply to the body.
Then wash it up with.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PLAGENTRA BABY BUBBLE WASH 
allantoin aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68988-080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	Allantoin	1.25 mg  in 250 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68988-080-01	250 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	04/01/2014

Labeler - C.A Pharm Co., Ltd. (688198385)

Registrant - C.A Pharm Co., Ltd. (688198385)

Establishment
Name	Address	ID/FEI	Business Operations
C.A Pharm Co., Ltd.		688198385	manufacture(68988-080)