Label: SERIOUS SKINCARE CONTINUOUSLY CLEAR ACNE MEDICATION FOR PROBLEMATIC SKIN DRY LO PRO ALL- OVER TREATMENT- salicylic acid lotion
- NDC Code(s): 53755-110-00
- Packager: Flageoli Limited
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 12, 2023
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- Drug Facts
- Active ingredient
- Uses
- Warnings
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Directions
- Shake before using. Apply the product on a cotton pad, then gently apply by tapping.
- Clean the skin thoroughly before applying this product.
- Cover the entire affected area with a thin layer one to three times daily.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
- If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
- Avoid contact with eyes, eyelids and mucous membranes.
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Inactive ingredients
Aqua (Water), Alcohol Denat., Allantoin, Citrus Grandis (Grapefruit) Fruit Extract, Dipotassium Glycyrrhizate, Calendula Officinalis Flower Extract, Salix Alba (Willow) Bark Extract, Sulfur, Centella Asiatica Extract, Propylene Glycol, Sodium Citrate, Methylpropanediol, PEG-40 Hydrogenated Castor Oil, PEG-6 Caprylic/capric Glycerides, Polysorbate 20, Zinc Oxide, Magnesium Aluminum Silicate, Caprylyl Glycol, Phenylpropanol, Pyridoxine HCl, Maltodextrin, Silica, Citric Acid, Parfum (Fragrance), Phenoxyethanol, Sodium Benzoate, Potassium Sorbate, Iron Oxides (CI 77491).
- Package Labeling:
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INGREDIENTS AND APPEARANCE
SERIOUS SKINCARE CONTINUOUSLY CLEAR ACNE MEDICATION FOR PROBLEMATIC SKIN DRY LO PRO ALL- OVER TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53755-110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) ALLANTOIN (UNII: 344S277G0Z) PUMMELO (UNII: ET1TN5W71X) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) SALIX ALBA BARK (UNII: 205MXS71H7) SULFUR (UNII: 70FD1KFU70) CENTELLA ASIATICA (UNII: 7M867G6T1U) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CITRATE (UNII: 1Q73Q2JULR) METHYLPROPANEDIOL (UNII: N8F53B3R4R) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8) POLYSORBATE 20 (UNII: 7T1F30V5YH) ZINC OXIDE (UNII: SOI2LOH54Z) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENYLPROPANOL (UNII: 0F897O3O4M) PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) MALTODEXTRIN (UNII: 7CVR7L4A2D) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53755-110-00 1 in 1 BOX 06/01/2018 1 200 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2018 Labeler - Flageoli Limited (036999498)