FDA.reportPublic FDA data

Solimo Repairing Treatment For Acne Prone Skin

Manufacturer
Amazon.com Services LLC | Filltech USA, LLC
Effective date
2023-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:21:13

Label at a glance#

ProductSolimo Repairing Treatment For Acne Prone Skin
Active ingredientBENZOYL PEROXIDE
Label structure7 sections

Indications and uses

for the management of acne

Dosage and administration

Apply product sparinglyto one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated below. Sensitivity Test for a New User: cleanse 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 t...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide 2.5%

Purpose

OTC - PURPOSE SECTION

Acne treatment gel

Uses

INDICATIONS & USAGE SECTION

  • for the management of acne

Warnings

WARNINGS SECTION

For external use only.

When using this product:

OTC - WHEN USING SECTION

  • do not use this product more than three times per day.
  • skin irritation and dryness are 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.
  • 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

OTC - DO NOT USE SECTION

if you

  • 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

DOSAGE & ADMINISTRATION SECTION

  • Apply product sparinglyto one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated below. Sensitivity Test for a New User:
  • cleanse 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.
  • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, ceteareth-20, propylene glycol, cetearyl alcohol, carbomer, ethoxydiglycol, cyclotetrasiloxane, glyceryl stearate, dimethicone, xanthan gum, peg-100 stearate, allantoin, panthenol, cyclopentasiloxane, fragrance, imidazolidinyl urea, methylparaben, propylparaben, sodium hydroxide.

Package Labeling:1oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:2oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2oz2oz

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72288-52572288-525-01, 72288-525-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
DIETHYLENE GLYCOL MONOETHYL ETHERA1A1I8X02BIACT
CYCLOMETHICONE 4CZ227117JEIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
DIMETHICONE92RU3N3Y1OIACT
XANTHAN GUMTTV12P4NEEIACT
PEG-100 STEARATEYD01N1999RIACT
ALLANTOIN344S277G0ZIACT
PANTHENOLWV9CM0O67ZIACT
CYCLOMETHICONE 50THT5PCI0RIACT
IMIDUREAM629807ATLIACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
SODIUM HYDROXIDE55X04QC32IIACT
BENZOYL PEROXIDEW9WZN9A0GMACTIB

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
2cd7e26e-4d76-9868-e063-6394a90a94fb19b9f227-d021-4b0e-a63d-93f3f9c3369c2025-01-29WarningsExact identifier
spl set id: 19b9f227-d021-4b0e-a63d-93f3f9c3369c

Reported adverse events (FAERS/openFDA)#

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