BP Spot Treatment

Manufacturer
Skin PS Brands | Cosmetic Solutions
Effective date
2021-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:43:09

Label at a glance#

ProductBP Spot Treatment
Active ingredientBENZOYL PEROXIDE
Label structure13 sections

Dosage and administration

clean 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 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 ...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide 10.0%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Use

INDICATIONS & USAGE SECTION

for the management of acne.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • 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 eyes, lips and mouth
  • avoid contact with hair and dyed fabrics, which may be bleached by 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.

Do not use if you

OTC - DO NOT USE SECTION

  • have very sensitive skin
  • are sensitive to Benzoyl Peroxide

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation becomes severe.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

INSTRUCTIONS FOR USE SECTION

  • clean 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 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.
  • Sensitivity Test for a New User:

​Apply product sparingly to one or two small affected areas during the first 3 days. if no discomfort occurs, follow the directions stated above.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Caprylic/Capric Triglyceride, Propanediol, Glycerin, Dimethicone, Glyceryl Oleate, Glyceryl Stearate, PEG-100 Stearate, Isosorbide Disunflowerseedate, Sodium Hyaluronate, Octyldodecyl PCA, Stearic Acid, Steareth-21, Cucumis Sativus Fruit Extract, Allantoin, Polysorbate 60, Sodium Citrate, Polyhydroxystearic Acid, Panethol, Carbomer, Titanium Dioxide, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Phenoxyethanol, Diethylhexyl Sodium Sulfosuccinate, Ethylhexylglycerin, Tocopheryl Acetate, Aluminum Stearate, Alumina, Sorbitan Isostearate, Citric Acid, Sodium Hydroxide.

How to use:

DOSAGE & ADMINISTRATION SECTION

Prep by cleansing skin. Apply a thin layer to the affected area. Reapply 1 to 3 times daily, as needed.

Questions or comments?

OTC - QUESTIONS SECTION

Visit us at slmdskincare.com

@slmdskincare

Distributed by Skin PS Brands

Culver City, CA 90232

Made in USA

SLMD Sandra Lee MD

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Skin Care by Dr. Pimple Popper

BP Spot Treatment

10% Benzoyl Peroxide

Acne Treatment

0.5 fl. oz. / 15 mL

Unit Carton:

BP Unit CartonBP Unit Carton

Primary Unit:

BP PrimaryBP Primary

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73318-1006-52023-09-12C16284748780-1f386c64a-28ec-0266-e053-dadaa90a7c1aBP Spot Treatment
73318-1006-52023-01-30C16284748780-1f386c64a-28ec-0266-e053-dadaa90a7c1aBP Spot Treatment

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73318-100673318-1006-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 33 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
052dfab4-692f-908e-e063-6294a90af871c44d2c3d-7332-4eb0-e053-2995a90aa3fb2023-09-12WarningsExact identifier
spl set id: c44d2c3d-7332-4eb0-e053-2995a90aa3fb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.