Label: SPECIAL CLEARING BOOSTER- benzoyl peroxide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 68479-503-00, 68479-503-02 - Packager: Dermalogica, Inc.
- Category: HUMAN OTC DRUG LABEL
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 November 23, 2015
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
When using this product,
- Avoid unnecessary sun exposure and use a sunscreen.
- Avoid contact with the eyes, lips, and mouth.
- This product may bleach hair or dyed products.
- Using other topical acne drugs at the same time or right after use of this product may increase dryness or irriatation of the skin.
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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 going outside, apply sunscreen after using this product. If irritation or sensativity develops, stop use of both products and ask a doctor.
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Inactive ingredients
Water/Aqua/Eau, PEG-8, Polysorbate 20, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Calendula Officinalis Flower Extract, Anthemis Nobilis Flower Extract, Tilia Cordata Flower Extract, Centaurea Cyanus Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Hypericum Perforatum Flower/Leaf/Stem Extract, Nasturtium Officinale Flower/Leaf Extract, Arctium Lappa Root Extract, Salvia Officinalis (Sage) Leaf Extract, Citrus Limon (Lemon) Fruit Extract, Hedera Helix (Ivy) Leaf/Stem Extract, Saponaria Officinalis Leaf/Root Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Cyclodextrin, Hydrolyzed Algin, Silica, Zinc Sulfate, Benzophenone-4, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Butylene Glycol,Disodium EDTA, Caprylyl Glycol, Chlorphenesin, Phenoxyethanol.
- Other information
- Questions or comments
- PRINCIPAL DISPLAY PANEL - 30 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
SPECIAL CLEARING BOOSTER
benzoyl peroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68479-503 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzoyl Peroxide (UNII: W9WZN9A0GM) (Benzoyl Peroxide - UNII:W9WZN9A0GM) Benzoyl Peroxide 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Polyethylene Glycol 400 (UNII: B697894SGQ) Polysorbate 20 (UNII: 7T1F30V5YH) Lavandula Angustifolia Flowering Top (UNII: 9YT4B71U8P) Calendula Officinalis Flower (UNII: P0M7O4Y7YD) Chamaemelum Nobile Flower (UNII: O2T154T6OG) Tilia Cordata Flower (UNII: CFN6G1F6YK) Centaurea Cyanus Flower (UNII: QZ239038YC) Chamomile (UNII: FGL3685T2X) St. John's Wort (UNII: UFH8805FKA) Nasturtium Officinale Flowering Top (UNII: W1N2U8I64G) Arctium Lappa Root (UNII: 597E9BI3Z3) Sage (UNII: 065C5D077J) Lemon (UNII: 24RS0A988O) Hedera Helix Leaf (UNII: ZP9XFG71A7) Saponaria Officinalis Leaf (UNII: 3988313MM7) Tea Tree Oil (UNII: VIF565UC2G) Silicon Dioxide (UNII: ETJ7Z6XBU4) Zinc Sulfate (UNII: 89DS0H96TB) Sulisobenzone (UNII: 1W6L629B4K) Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked) (UNII: 59TL3WG5CO) Aminomethylpropanol (UNII: LU49E6626Q) Butylene Glycol (UNII: 3XUS85K0RA) Edetate Disodium (UNII: 7FLD91C86K) Caprylyl Glycol (UNII: 00YIU5438U) Chlorphenesin (UNII: I670DAL4SZ) Phenoxyethanol (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68479-503-02 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:68479-503-00 2 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333D 09/22/2011 Labeler - Dermalogica, Inc. (177698560) Establishment Name Address ID/FEI Business Operations PakLab 790530976 MANUFACTURE(68479-503) Establishment Name Address ID/FEI Business Operations Diamond Wipes 161104729 MANUFACTURE(68479-503)