Label: DERMALL MATRIX EYE ZONE DERMAL CARE MASK- adenosine patch
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Contains inactivated NDC Code(s)
NDC Code(s): 72371-020-01, 72371-020-02 - Packager: Rion MediFab 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 July 6, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water, Collagen Extract, Glycerin, Chondrus Chrispus Powder, Ceratonia Siliqua Gum, Xanthan Gum, Butylene Glycol, Calcium Chloride, Amino acid complex, Hydrolized collagen, Coix Lacryma-Jobi Ma-yuen Seed Extract, Oryza Sativa(Rice) Bran Extact, Red Ginseng Extract, Argania Spinosa Kernel Oil, Adenosine, PEG-60 Hydrogenated Caster Oil, Disodium EDTA, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Houttuynia Cordata Extract, Artemisia Vulgaris Extract, Citrus Junos Fruit Extract, 1,2-Hexanediol, Caprylyl Glycol, Ethyl Hexanediol, Citrus Grandis (Grapefruit) Seed Extract, Bambusa Textilis Stem Extract, Pinus Palustris Leaf Extract, Chlorphenesin, Phenoxyethanol, Methylparaben, Fragrance
- PURPOSE
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WARNINGS
Warnings:
1. Avoid using on blemishes, pimples, irritated or sunburned skin 2. Avoid using on skin which is sensitive to bandages, tapes or peel-off masks. 3. Stop using if skin becomes reddish, swollen or itchy, during and after usage. 4. Avoid contact with eyes directly. 5. For external use only. Keep out of reach of children. 6. Avoid severe stimulation when you attach biogel sheets. 7. Once opened, use biogel sheet immediately.
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DERMALL MATRIX EYE ZONE DERMAL CARE MASK
adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72371-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.001 g in 2.8 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72371-020-02 8 in 1 CARTON 05/01/2018 1 NDC:72371-020-01 2.8 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2018 Labeler - Rion MediFab Inc. (690056695) Registrant - Rion MediFab Inc. (690056695) Establishment Name Address ID/FEI Business Operations JT Co., Ltd. 557785196 manufacture(72371-020)
