Label: YES TO TOMATOES ACNE FIGHTING MIST- salicylic acid spray
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Contains inactivated NDC Code(s)
NDC Code(s): 69840-017-08 - Packager: Yes To Incorporated
- 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
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
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Directions
- 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.
- Close eyes and press down on pump to mist your way to clear skin!
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Inactive Ingredients
Aloe Barbadensis Leaf Juice, Alcohol Denatured, Water (Aqua), Pentylene Glycol, Polyglyceryl-4 Laurate/Sebacate, Polyglyceryl-4 Caprylate/Caprate, Propanediol, Biosaccharide Gum-1, Caprylyl/Capryl Glucoside, Hamamelis Virginiana (Witch Hazel) Water, Glycerin, Solanum Lycopersicum (Tomato) Fruit Extract, Niacinamide, Disodium EDTA, Sodium Hydroxide, Fragrance (Parfum), Benzyl Benzoate, Coumarin, Butylphenyl methylpropional.
- Questions?
- PRINCIPAL DISPLAY PANEL - 30 mL Bottle Label
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INGREDIENTS AND APPEARANCE
YES TO TOMATOES ACNE FIGHTING MIST
salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69840-017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Pentylene Glycol (UNII: 50C1307PZG) Polyglycerin-4 (UNII: YX76MGM96B) Polyglyceryl-4 Caprate (UNII: 3N873UN885) GLYCERIN (UNII: PDC6A3C0OX) Biosaccharide Gum-1 (UNII: BB4PU4V09H) Caprylyl/Capryl Oligoglucoside (UNII: E00JL9G9K0) Witch Hazel (UNII: 101I4J0U34) Niacinamide (UNII: 25X51I8RD4) Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM) PROPANEDIOL (UNII: 5965N8W85T) ALOE VERA LEAF (UNII: ZY81Z83H0X) Alcohol (UNII: 3K9958V90M) SOLANUM LYCOPERSICUM FRUITING TOP (UNII: X636CG4BH0) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69840-017-08 30 mL in 1 BOTTLE, SPRAY; 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 Incorporated (788689680) Establishment Name Address ID/FEI Business Operations Emilia Resources Limited 079378421 MANUFACTURE(69840-017)