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Biellee Pollen Whitening Wrinkle Time Repair Ampoule

Medically reviewed on Jun 21, 2018

Dosage form: cream
Ingredients: GLYCERIN 1.2mg in 10mL
Labeler: NSB CO., LTD.
NDC Code: 70784-001

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Facts

GLYCERIN 12.00%

Skin Protectant

Temporarily protects chapped or cracked skin
Prevent and protect from the drying effects of wind and cold weather

Apply liberally as needed onto clean facial skin day or night
Children under 6 months: ask a doctor

For external use only

Do not use on damaged or broken skin

When using this product, keep out of eyes. Rinse with water to remove.

Stop using and ask a doctor if rash occurs.

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

WATER
POLLEN EXTRACT
DIPROPYLENE GLYCOL
BUTYLENE GLYCOL
MORINDA CITRIFOLIA FRUIT EXTRACT
ALCOHOL
NIACINAMIDE
PHENOXYETHANOL
FRAGRANCE
PEG-40 HYDROGENATED CASTOR OIL
PPG-26-BUTETH-26
CARBOMER
XANTHAN GUM
ALLANTOIN
SODIUM HYALURONATE
POTASSIUM HYDROXIDE
ETHYLHEXYLGLYCERIN
DISODIUM EDTA

BIELLEE POLLEN WHITENING WRINKLE TIME REPAIR AMPOULE 
glycerin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70784-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN1.2 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
BEE POLLEN 
DIPROPYLENE GLYCOL 
BUTYLENE GLYCOL 
NONI FRUIT 
ALCOHOL 
NIACINAMIDE 
PHENOXYETHANOL 
POLYOXYL 40 HYDROGENATED CASTOR OIL 
PPG-26-BUTETH-26 
CARBOXYPOLYMETHYLENE 
XANTHAN GUM 
ALLANTOIN 
HYALURONATE SODIUM 
POTASSIUM HYDROXIDE 
ETHYLHEXYLGLYCERIN 
EDETATE DISODIUM 
Packaging
#Item CodePackage Description
1NDC:70784-001-023 CONTAINER in 1 CARTON
1NDC:70784-001-0110 mL in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/21/2016
Labeler - NSB CO., LTD. (689846922)
Registrant - NSB CO., LTD. (689846922)
Establishment
NameAddressID/FEIOperations
NSB CO., LTD.689846922manufacture(70784-001)

 
NSB CO., LTD.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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