OTC Medication Information: SUPER CREAM AGE CONTROL AND FIRMING

SUPER CREAM AGE CONTROL AND FIRMING- dimethicone cream
UNHWA CORPORATION

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: DIMETHICONE

Inactive Ingredients:
Water, Cyclopentasiloxane, Propanediol, Dipropylene Glycol, Caprylic/Capric Triglyceride, Hydrogenated Polydecene, Mineral Oil, Cetearyl Alcohol,
Betaine, Glyceryl Stearate SE, Sodium Hyaluronate, Polyglyceryl-3 Methylglucose Distearate, Caprylyl Methicone, Beeswax, Glyceryl Stearate, PEG-100 Stearate,
Trehalose, Panax Ginseng Cambium Cell Culture Extract, Alcohol, Cetearyl Olivate, Sorbitan Olivate, Sodium Polyacrylate, Caprylyl Glycol,
Ethylhexylglycerin, Fragrance, Trideceth-6, Tocopheryl Acetate, Panthenol, Hydrolyzed Collagen, Ethylhexyl Stearate, Dipotassium Glycyrrhizate,
Dimethicone/Vinyl Dimethicone Crosspolymer, Citrus Paradisi (Grapefruit) Fruit Extract, Sophora Angustifolia Root Extract,
Eugenia Caryophyllus (Clove) Flower Extract, Eucalyptus Globulus Leaf Extract, Citrus Junos Fruit Extract, Glycerin, Allantoin, Adenosine,
Xanthan Gum, Palmitoyl Tripeptide-5, Disodium EDTA

Direction for Use: Dab a small amount and smooth evenly working around the eyes from under the eyes to eyelids in circular motion. Lightly tap around the eyes for absorption.
Storage: Store in cool and dry place.
Warning: For external use only. Should any abnormality appear, stop usage of the product and consult doctor.

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SUPER CREAM AGE CONTROL AND FIRMING
dimethicone cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50556-004
Route of Administration CUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIMETHICONE (DIMETHICONE) DIMETHICONE 0.58 mL in 45 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50556-004-01 45 mL in 1 CARTON None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part347 10/01/2009
Labeler — UNHWA CORPORATION (688202545)

Revised: 05/2010 UNHWA CORPORATION

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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