Label: ACNE CONTROL SERUM- benzoyl peroxide lotion
- NDC Code(s): 72957-001-01
- Packager: Private Label Skin Care
- This is a repackaged label.
- Source NDC Code(s): 39765-030
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 26, 2025
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use if you • have very sensitive skin • are sensitive to benzoyl peroxide
When using this product • skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration • 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 • avoid unnecessary sun exposure and use a sunscreen • avoid contact with the eyes, lips, and mouth • avoid contact with hair and dyed fabrics, which may be bleached by this product
Stop use and ask a doctor if • irritation becomes severe
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Directions
• wash the skin thoroughly before applying this product • Apply affected area with a thin layer, avoiding eye area • Allow to absorb before applying additional products. • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two 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 • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor
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Inactive ingredients
Water/Aqua/Eau, Glycolic Acid, Sclerotium Gum, Arnica (Arnica Montana) Flower Extract, Calendula (Calendula Officinalis) Flower Extract, ConeFlower (Echinacea Purpurea) Extract, Goldenseal (Hydrastis Canadensis) Extract, Lavender (Lavandula Angustifolia) Flower Extract, Gluconolactone, Sodium Hydroxide, Sodium Benzoate, Allantoin, Tetrasodium EDTA, Glycerin
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
ACNE CONTROL SERUM
benzoyl peroxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72957-001(NDC:39765-030) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCOLIC ACID (UNII: 0WT12SX38S) BETASIZOFIRAN (UNII: 2X51AD1X3T) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98) GOLDENSEAL (UNII: ZW3Z11D0JV) LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) GLUCONOLACTONE (UNII: WQ29KQ9POT) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM BENZOATE (UNII: OJ245FE5EU) ALLANTOIN (UNII: 344S277G0Z) EDETATE SODIUM (UNII: MP1J8420LU) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72957-001-01 32 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 01/23/2020 Labeler - Private Label Skin Care (116996962) Establishment Name Address ID/FEI Business Operations Private Label Skin Care 116996962 relabel(72957-001)
