Label: CELDERMA PEARL LACE HYDROGEL MASK- glycerin,niacinamide, adenosine patch
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Contains inactivated NDC Code(s)
NDC Code(s): 72044-104-01, 72044-104-02 - Packager: GENIC CO., LTD
- 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 March 20, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use when skin is red, inflamed, irritated, or painful
When using this product
- do not apply on other parts of the body
- do not use on damaged or broken skin
- avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
- do not apply directly to wound or open cut
Stop use and ask a doctor if
- Rash or irritation on skin develops and lasts
- Keep out of reach of children
- Directions
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Inactive ingredients
Water, Ceratonia Siliqua (Carob) Gum, Chondrus Crispus (Carrageenan) Extract, Phenoxyethanol, PEG-60 Hydrogenated Castor Oil, Polyacrylate-13, Allantoin, Scutellaria Baicalensis Root Extract, Pearl Extract (796ppm), Ethylhexylglycerin, Polyisobutene, 1,2-Hexanediol, Camellia Sinensis Leaf Extract, Artemisia Princeps Leaf Extract, Houttuynia Cordata Extract, Caprylyl Glycol, Sodium Polyacrylate, Synthetic Fluorphlogopite, Butylene Glycol, Disodium EDTA, Fragrance, Lactobacillus Ferment, Citrus Junos Fruit Extract, Polysorbate 20, Ricinus Communis (Castor) Seed Oil, Sorbitan Isostearate, Titanium Dioxide (CI 77891), Polymethylsilsesquioxane, Caesalpinia Spinosa Fruit Extract, Potassium Hydroxide, Tin Oxide (CI 77861), Kappaphycus Alvarezii Extract, Diamond powder (1ppm)
- CELDERMA Pearl Lace Hydrogel Mask
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INGREDIENTS AND APPEARANCE
CELDERMA PEARL LACE HYDROGEL MASK
glycerin,niacinamide, adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72044-104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.012 g in 30 g NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 0.6 g in 30 g GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 6 g in 30 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALLANTOIN (UNII: 344S277G0Z) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG) HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72044-104-02 1 in 1 POUCH 03/20/2018 1 NDC:72044-104-01 30 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/20/2018 Labeler - GENIC CO., LTD (688483171) Registrant - GENIC CO., LTD (688483171) Establishment Name Address ID/FEI Business Operations GENIC CO.,LTD 688483171 manufacture(72044-104)