Label: YES TO TOMATOES ACNE FIGHTING SCRUB AND CLEANSER- salicylic acid suspension
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Contains inactivated NDC Code(s)
NDC Code(s): 69840-015-06 - Packager: Yes To, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 29, 2019
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
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Directions
- gently massage the scrub onto damp skin in a circular motion
- clean the skin by covering the entire affected area with a thin layer and rinse thoroughly 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.
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Inactive Ingredients
(Aqua), Sodium Cocoyl Glutamate, Propanediol, Glycerin, Sodium Coco-Sulfate, Xanthan Gum, Polylactic Acid, Solanum Lycopersicum (Tomato) Fruit Extract, Hamamelis Virginiana (Witch Hazel) Water, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Aspalathus Linearis Extract, Chamomilla Recutita (Matricaria) Extract, Cucurbita Pepo (Pumpkin) Fruit Extract, Ginkgo Biloba Leaf Extract, Glyceryl Caprylate, Tetrasodium Glutamate Diacetate, Hydrogenated Jojoba Oil, Caprylhydroxamic Acid, Glyceryl Undecylenate, Alcohol, Benzoic Acid, Fragrance (Parfum), Benzyl Benzoate.
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- PRINCIPAL DISPLAY PANEL - 85 g Tube Label
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INGREDIENTS AND APPEARANCE
YES TO TOMATOES ACNE FIGHTING SCRUB AND CLEANSER
salicylic acid suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69840-015 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) PROPANEDIOL (UNII: 5965N8W85T) GLYCERIN (UNII: PDC6A3C0OX) SODIUM COCO-SULFATE (UNII: 3599J29ANH) XANTHAN GUM (UNII: TTV12P4NEE) POLYLACTIDE (UNII: 459TN2L5F5) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) SOLANUM LYCOPERSICUM (UNII: 0243Q4990L) TEA TREE OIL (UNII: VIF565UC2G) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544) ALCOHOL (UNII: 3K9958V90M) ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU) MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) PUMPKIN (UNII: SYW0QUB89Y) GINKGO (UNII: 19FUJ2C58T) BENZOIC ACID (UNII: 8SKN0B0MIM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69840-015-06 85 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product 06/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/01/2019 Labeler - Yes To, Inc. (788689680)