Label: DERMAHEAL SKIN DELIGHT MASK PACK PLUS (copper tripeptide-1- 0.001% patch
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Contains inactivated NDC Code(s)
NDC Code(s): 60709-106-01 - Packager: YBK Investment, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 Label Information
Updated November 1, 2013
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Skin Delight Mask Plack Plus
Purpose
Replenishes dry and dull skin
Brightens and makes even skin tone using innovative biomimetic peptides
Direction for Use
Apply mask to clean face. Leave the mask on your face about 15-20 minutes until it begins to dry.
Caution
For external use only, not to be swallowed
In case of accidental ingestion, seek professional assistance.
Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and consult a doctor if rash or irritation develops and lasts.
Do not apply directly to wound or open cut.
Keep out of reach of children
Store at room temperature
Purpose
Replenishes dry and dull skin
Brightens and makes even skin tone using innovative biomimetic peptides
Water(Aqua), Glycerin, Butylene Glycol, Hydrolyzed Collagen, Camellia Sinensis Leaf Extract, Beta-Glucan, Morus Alba Bark Extract, Xanthan Gum, Arbutin, Phenoxyethanol, 3-o-Ethyl Ascorbic Acid, Polysorbate 80, Glycine Soja(Soybean) Oil, Hydrogenated Lecithin, Panthenol, Sodium Hyaluronate, Disodium EDTA, Fragrance(Parfum), PALMITOYL OLIGOPEPTIDE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
DERMAHEAL SKIN DELIGHT MASK PACK PLUS
copper tripeptide-1 (0.001%) patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60709-106 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PREZATIDE COPPER (UNII: 6BJQ43T1I9) (PREZATIDE COPPER - UNII:6BJQ43T1I9) PREZATIDE COPPER 0.22 mg in 22 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAMELLIA SINENSIS VAR. ASSAMICA WHOLE (UNII: 6ZU7I0L9K2) MORUS ALBA BARK (UNII: 7O71A48NDP) XANTHAN GUM (UNII: TTV12P4NEE) ARBUTIN (UNII: C5INA23HXF) PHENOXYETHANOL (UNII: HIE492ZZ3T) 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) POLYSORBATE 80 (UNII: 6OZP39ZG8H) SOYBEAN OIL (UNII: 241ATL177A) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) PANTHENOL (UNII: WV9CM0O67Z) HYALURONATE SODIUM (UNII: YSE9PPT4TH) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60709-106-01 22 g in 1 PATCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/21/2013 Labeler - YBK Investment, INC (010397213) Registrant - YBK Investment, INC (010397213) Establishment Name Address ID/FEI Business Operations Caregen Co., Ltd. 689850365 manufacture(60709-106)