Label: AN ADC SP F- adenosine solution
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Contains inactivated NDC Code(s)
NDC Code(s): 69153-070-01, 69153-070-02 - Packager: AN 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 June 24, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
SP F I) Inactive Ingredients: Water, Carbomer, Beta-Glucan, Caffeine, Avena Sativa (Oat) Kernel Extract, Hovenia Dulcis Fruit Extract, Centella Asiatica Extract/Diospyros Kaki Leaf Extract/Theobroma Cacao Extract/Chamomilla Recutita (Matricaria) Extract/Wine Extract, Glycine Soja (Soybean) Seed Extract, Origanum Vulgare Flower Extract, Octanediol (Carprylyl Glycol), Phenoxyethanol, Phenoxyethanol, Sophora Flavescens Root Extract, Scutellaria Baicalensis Root Extract, Acetyl Hexapeptide-8, Copper Tripeptide-1
SP F II) Inactive Ingredients: Sodium Silicate / Hydroxypropyl Chitosan, Water, Ipomoea Purpurea Extract/Paeonia Albiflora Flower Extract/Magnolia Liliflora Flower Extract/Lilium Candidum Flower Extract, Sodium Hydroxide, Camellia Sinensis Leaf Extract, Portulaca Oleracea Extract, Polyepsilon-Lysine
- PURPOSE
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WARNINGS
Precautions on use: 1. Stop using the product if there are any of the following abnormal symptoms appearing after use and consult with your dermatologist as continued use can worsen the symptoms. A) If there are red spots, swelling, itchiness, or irritation B) If the above symptoms appear around the skin to which the product has been applied after being exposed to direct sunlight. 2. Precautions on storage and handling A) Make sure to close the cap after use. B) Keep out of the reach of children. C) Do not keep the product in a hot or cold place or a place getting direct sunlight. 3. Do not apply the product to any parts of the skin with wound, eczema, or dermatitis.
- KEEP OUT OF REACH OF CHILDREN
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Suggested use and application order
Suggested use and application order: 1. Open SP F Ⅰ until the dotted line. (try not to spill the liquid content inside) 2. Open SP F Ⅱ and mix with SP F Ⅰ. (try not to spill the liquid content inside) 3. Seal the package of SP F Ⅰ and strongly shake the package more than 10 times to mix two agents well. (turning into gel when mixed enough) 4. Apply the content over your face enough with a brush contained inside the package. 5. Regardless of individual difference, wait for 15 ~ 20 minutes. (gently fan yourself while waiting) Try not to move or speak. 6. For the first few times, your skin may feel strongly stretched and there is a difference in color change depending on area. (discharge of toxin out of the skin) Feeling of stretching may differ by individual skin condition. 7. After enough application, wash your face with warm water and then use soap to cleanse your face once again. 8. Dry your face with a dry towel.
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AN ADC SP F
adenosine solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69153-070 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 2.8 mg in 7 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69153-070-02 10 in 1 CARTON 05/01/2016 1 NDC:69153-070-01 7 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2016 Labeler - AN Co Ltd. (688448454) Registrant - AN Co Ltd. (688448454) Establishment Name Address ID/FEI Business Operations AN Co Ltd. 688448454 manufacture(69153-070)