Label: CLEARASIL ULTRA RAPID ACTION SCRUB- salicylic acid lotion
- NDC Code(s): 63824-416-65
- Packager: RB Health (US) LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 6, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only
When using this product
- avoid contact with the eyes. If the product gets into the eyes, rinse thoroughly with water.
- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
- limit use to the face and neck
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Directions
- wet face
- dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area
- cover the entire affected area with a thin layer and rinse thoroughly with warm water 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 occurs, reduce application to once a day or every other day
- Other information
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Inactive ingredients
water, polyethylene, PPG-15 stearyl ether, glycerin, stearyl alcohol, cetyl betaine, distearyldimonium chloride, sodium lauryl sulfate, cetyl alcohol, alcohol, steareth-21, sodium chloride, behenyl alcohol, synthetic wax, steareth-2, fragrance, Lavandula stoechas extract, Helichrysum italicum extract, Cistus monspeliensis extract, xanthan gum, dimethyl palmitamine, lauryl alcohol, mica, isopropyl alcohol, disodium EDTA, BHT, magnesium nitrate, methylchloroisothiazolinone, magnesium chloride, methylisothiazolinone, sodium sulfate, ferric ferrocyanide, titanium dioxide, FD&C blue no. 1
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 150 mL Tube Label
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INGREDIENTS AND APPEARANCE
CLEARASIL ULTRA RAPID ACTION SCRUB
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-416 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 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) GLYCERIN (UNII: PDC6A3C0OX) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CETYL BETAINE (UNII: E945X08YA9) DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X) SODIUM LAURYL SULFATE (UNII: 368GB5141J) CETYL ALCOHOL (UNII: 936JST6JCN) ALCOHOL (UNII: 3K9958V90M) STEARETH-21 (UNII: 53J3F32P58) SODIUM CHLORIDE (UNII: 451W47IQ8X) DOCOSANOL (UNII: 9G1OE216XY) STEARETH-2 (UNII: V56DFE46J5) LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A) HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24) XANTHAN GUM (UNII: TTV12P4NEE) DIMETHYL PALMITAMINE (UNII: 5E4QI660PW) LAURYL ALCOHOL (UNII: 178A96NLP2) MICA (UNII: V8A1AW0880) ISOPROPYL ALCOHOL (UNII: ND2M416302) EDETATE DISODIUM (UNII: 7FLD91C86K) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) MAGNESIUM NITRATE (UNII: 77CBG3UN78) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SODIUM SULFATE (UNII: 0YPR65R21J) FERRIC FERROCYANIDE (UNII: TLE294X33A) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63824-416-65 150 mL in 1 TUBE; Type 0: Not a Combination Product 12/01/2013 09/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 12/01/2013 09/01/2024 Labeler - RB Health (US) LLC (081049410)
