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PLAGENTRA MOTHERS BELLY by C.A Pharm Co., Ltd.

Medically reviewed on December 5, 2017

Dosage form: oil
Ingredients: Allantoin 0.75mg in 150mL
Labeler: C.A Pharm Co., Ltd.
NDC Code: 68988-030

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ACTIVE INGREDIENT

Active Ingredient: Allantoin 0.5%

INACTIVE INGREDIENT

Inactive Ingredients:
Ethylhexyl Palmitate, Caprylic/Capric Triglyceride, Vitis Vinifera (Grape) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Olea Europaea (Olive) Fruit Oil, Macadamia Integrifolia Seed Oil, Limnanthes Alba (Meadowfome) Seed Oil, Tocopheryl Acetate, Copper Tripeptide-1, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Palmitoyl pentapeptide-4

PURPOSE

Purpose: Skin Protectant

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 after shower.

DOSAGE & ADMINISTRATION

Dosage and administration:
Massage the Belly Oil into the stretch marks and the surrounding area.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PLAGENTRA MOTHERS BELLY 
allantoin oil
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68988-030
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Allantoin (ALLANTOIN) Allantoin0.75 mg  in 150 mL
Inactive Ingredients
Ingredient NameStrength
Ethylhexyl Palmitate 
GRAPE SEED OIL 
Packaging
#Item CodePackage Description
1NDC:68988-030-01150 mL in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34704/01/2014
Labeler - C.A Pharm Co., Ltd. (688198385)
Registrant - C.A Pharm Co., Ltd. (688198385)
Establishment
NameAddressID/FEIOperations
C.A Pharm Co., Ltd.688198385manufacture(68988-030)

 
C.A Pharm Co., Ltd.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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