Tinted Acne Treatment

Manufacturer
Walgreens | Product Quest Mfg.
Effective date
2018-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:19

Label at a glance#

ProductTinted Acne Treatment
Active ingredientResorcinol, Sulfur
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                                                                 Purpose
Resorcinol - 2.00%...............................................................................................Acne Treatment
Sulfur - 8.00% .................................................................................................... Acne Treatment

INDICATIONS & USAGE SECTION

Use for the treatment of acne

WARNINGS SECTION

Warnings
For external use only
Do not use • if you have very sensitive skin or are sensitive to benzoyl peroxide
When using this product • 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. • rinse right away with water if it gets in eyes • avoid unnecessary sun exposure and use a sunscreen • avoid contact with the eyes, lips, and mouth • 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.
Stop use and ask a doctor if skin irritation becomes severe

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions • cleanse the skin thoroughly before applying medication • cover the entire affected area
with a thin layer one to three times a day • 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, use a sunscreen. Allow product to dry, then follow direction in the sunscreen labeling. If
sensitivity develops, discontinue use of both products and consult a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Alcohol Denat.
Bentonite
Fragrance
Glyceryl Stearate SE
Iron Oxides
Isopropyl Myristate
Methylparaben
Propylene Glycol
Propylparaben
Simethicone
Titanium Dioxide
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312793resorcinol 2 % / sulfur 8 % Topical CreamPSN1
312793resorcinol 20 MG/ML / sulfur 80 MG/ML Topical CreamSCD1
312793resorcinol 2 % / sulfur 8 % Topical CreamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-7783-012020-01-31C16284748780-19d75b9cf-f9fe-f424-e053-dadaa90a57ceWell at Walgreens Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-7783-01Tinted Acne Treatment1 in 1 CARTONCREAM11
0363-7783-01Tinted Acne Treatment18 g in 1 TUBECREAM181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-7783TINTED ACNE TREATMENT (RESORCINOL 2.00% SULFUR 8.00%) CREAM [WALGREENS]1Legacy NDC, 2 package rows20180501_30e7d8f7-ca10-436a-8cce-25f97a7163a9.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-77830363-7783-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
3e34a4b1-8e84-4968-9ba3-9e29d026671830e7d8f7-ca10-436a-8cce-25f97a7163a92018-05-01WarningsExact identifier
spl id: 3e34a4b1-8e84-4968-9ba3-9e29d0266718
spl set id: 30e7d8f7-ca10-436a-8cce-25f97a7163a9

Reported adverse events (FAERS/openFDA)#

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