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Dosage form: cream
Ingredients: GLYCERIN 0.04g in 1mL
Labeler: IASO Inc
NDC Code: 75847-1705

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.

Drug Facts


water, diospyros kaki leaf ext, pinus densiflora leaf ext, cyclopentasiloxane, glycerin, dimethicone, betaine, c6-14 olefin, cyclomethicone, dimethicone/vinyl dimethicone crosspolymer, petrolatum, glyceryl stearate, peg-100 stearate, cetyl alcohol, shea butter, piper methysticum leaf/root/stem ext, portulaca oleracea ext, bisabolol, soluble collagen, pueraria thunbergiana root ext, peg/ppg-18/18 dimethicone, sodium polyacrylate, methylparaben, algae ext, cnidium officinale root ext, licorice root ext, paeonia lactiflora root ext, hydrogenated lecithin, argania spinosa kernel oil, phenoxyethanol, aloe barbadensis leaf juice, polysorbate 20, trideceth-6, fragrance, buddleja axillaris leaf ext, althaea rosea flower ext, propylparaben, dicaprylyl carbonate, sodium hyaluronate, benzophenone-4, sucrose distearate, polyglutamic acid, butylparaben, ceramide 3, ethylparaben, butylene glycol, tocopheryl acetate, xanthan gum, folic acid, polyquaternium-51, cholesterol, raffinose, alcohol, tromethamine, acetyl glucosamine, ascorbyl glucoside, niacinamide, plamitoyl pentapeptide-4, panthenol, ethoxydiglycol

skin whitening

keep out of reach of the children

apply in the morning and evening, as the last step of your skin care program, apply a small amount to the face and neck

- Stop using if sensitivities occurs and consult with dermatologist
- sensitivities such as red marks, intumescence, urtication, irritation during use
-Have sensitivities as above on applied part by direct sun ray
- Do not store at high and low temperatures and avoid sunlight.

for external use only

glycerin cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75847-1705
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:75847-1705-145 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34708/01/2013
Labeler - IASO Inc (688771690)
Registrant - IASO Inc (688771690)
Kolmar Korea Co., Ltd687846360manufacture(75847-1705)

Revised: 08/2013

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.