Label: DR YOUNG AC CONTROL U LINE CLEARING MIST- salicylic acid spray
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Contains inactivated NDC Code(s)
NDC Code(s): 43948-1350-1, 43948-1350-2 - Packager: Tdc, 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 December 5, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Dipropylene Glycol, Alcohol, Chrysanthellum Indicum Extract, Fomes Officinalis(Mushroom) Extract, Oleanolic Acid, Enantia Chlorantha Bark Extract, Butylene Glycol, Diospyros Kaki Leaf Extract, Rhus Semialata Gall Extract, Betula Platyphylla Japonica Bark Extract, Glycerin, Trehalose, PPG-26- Buteth-26, PEG-40 Hydrogenated Castor Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Zinc Sulfate, Citrus Limon (Lemon) Fruit Extract, Methylparaben
- PURPOSE
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WARNINGS
Warning: 1) For external use only. 2) Using other topical acne medications at the same time or immediately following the use of this product may increase dryness or irritation of the skin. 3) If this occurs, only one drug should be used unless directed by a doctor. 4) Avoid direct contact with eyes. 5) If contact occurs, flush thoroughly with water. 6) If swallowed, get medical help or contact a Poison Control Center right away. 7) Not to be used for children under 3 years of age.
Storage and cautions for handling: 1) Keep out of reach of children. 2) Keep away from high or low temperature and direct sunlight.
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR YOUNG AC CONTROL U LINE CLEARING MIST
salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43948-1350 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid 0.14 g in 140 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Dipropylene Glycol (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43948-1350-2 1 in 1 CARTON 10/01/2017 1 NDC:43948-1350-1 140 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2017 Labeler - Tdc, Co. Ltd (687479378) Registrant - Tdc, Co. Ltd (687479378) Establishment Name Address ID/FEI Business Operations Biocostec Co., Ltd. 690407325 manufacture(43948-1350)
