Label: BUBBLE FADE AWAY ACNE SPOT TREATMENT- benzoyl peroxide emulsion
- NDC Code(s): 83509-003-01
- Packager: BUBBLE BEAUTY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 20, 2025
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only.
When using this product
- skin irritation or dryness may occur if you use another topical acne medication at the same time. If irritation occurs, use one 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
- redness, burning, itching, peeling, or possibly swelling may occur. Irritation may be reduced by using the product less or in a lower concentration.
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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.
- Other information
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Inactive ingredients
Water (Aqua), Glycerin, Propanediol, Carbomer, Glycyrrhiza Glabra (Licorice) Root Extract, Niacinamide, Allantoin, Zinc Pca, Laureth-4, Xanthan Gum, Aloe Barbadensis Leaf Juice, Diethylhexyl Sodium Sulfosuccinate, Sambucus Nigra Fruit Juice, Spiraea Ulmaria Flower Extract, Sodium Hydroxide, Sodium Citrate, Sodium Phytate, Potassium Sorbate, Citric Acid, Sodium Benzoate, Sodium Sulfite
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- Product Packaging
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INGREDIENTS AND APPEARANCE
BUBBLE FADE AWAY ACNE SPOT TREATMENT
benzoyl peroxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83509-003 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 SODIUM PHYTATE (UNII: 88496G1ERL) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) GLYCYRRHIZA GLABRA (LICORICE) ROOT (UNII: 2788Z9758H) NIACINAMIDE (UNII: 25X51I8RD4) ALLANTOIN (UNII: 344S277G0Z) ZINC PCA (UNII: C32PQ86DH4) LAURETH-4 (UNII: 6HQ855798J) XANTHAN GUM (UNII: TTV12P4NEE) DIETHYLHEXYL SODIUM SULFOSUCCINATE (UNII: F05Q2T2JA0) ALOE VERA LEAF (UNII: ZY81Z83H0X) SAMBUCUS NIGRA FRUIT JUICE (UNII: Z4IFJ0AK1E) FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) CARBOMER (UNII: 0A5MM307FC) GLYCERIN (UNII: PDC6A3C0OX) PROPANEDIOL (UNII: 5965N8W85T) SODIUM SULFITE (UNII: VTK01UQK3G) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83509-003-01 1 in 1 CARTON 12/01/2024 1 10 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 12/01/2024 Labeler - BUBBLE BEAUTY (117396016)