Label: ACNE CLEARING TONER- salicylic acid liquid
- NDC Code(s): 84262-011-01
- Packager: GLYTONE LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 28, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Use
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Warnings
For external use only.
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Directions
- After cleansing, apply toner to a cotton pad and gently apply over affected area one to three times daily.
- Do not rinse.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to 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 toher day.
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACNE CLEARING TONER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84262-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) ICODEXTRIN (UNII: 2NX48Z0A9G) GLYCERIN (UNII: PDC6A3C0OX) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) APPLE (UNII: B423VGH5S9) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SAW PALMETTO (UNII: J7WWH9M8QS) AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777) MANDELIC ACID (UNII: NH496X0UJX) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM HYDROXIDE (UNII: 55X04QC32I) POLYDEXTROSE (UNII: VH2XOU12IE) EPILOBIUM FLEISCHERI WHOLE (UNII: 8E2KLS8J8K) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) SODIUM BENZOATE (UNII: OJ245FE5EU) PROPANEDIOL (UNII: 5965N8W85T) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) NIACINAMIDE (UNII: 25X51I8RD4) ALLANTOIN (UNII: 344S277G0Z) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SALIX ALBA BARK (UNII: 205MXS71H7) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84262-011-01 1 in 1 CARTON 03/01/2024 1 240 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 03/01/2024 Labeler - GLYTONE LLC (119226548) Registrant - GLYTONE LLC (119226548)