Spot Acne Treatment

Manufacturer
Walgreens | Product Quest Mfg
Effective date
2018-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:18

Label at a glance#

ProductSpot Acne Treatment
Active ingredientSalicylic Acid
Label structure6 sections

Dosage and administration

Cleanse thoroughly before applying treatment Cover the entire affected area with a thin layer one to three times daily. Because of excessive drying of the skin may occurs, 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 usage to once a day or every other day.

Label contents#

Full prescribing information#

Active ingredients                 Purpose

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid - 2.0%              Acne Medication 

Use

INDICATIONS & USAGE SECTION

Helps prevent new acne blemishes

For external use onlyFlammable, keep away from oipen fire or flame

WARNINGS SECTION

When using this product skin irritation and dryness is more likely occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Avoid contact with eyes. If contact occurs, flush thoroughly with water

SPL UNCLASSIFIED SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Cleanse thoroughly before applying treatment
Cover the entire affected area with a thin layer one to three times daily.
Because of excessive drying of the skin may occurs, 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 usage to once a day or every other day.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol
Ammonium Hydroxide
Benzalkonium Chloride
Butylene Glycol
C12-15 Alkyl Lactate
C13-14 Isoparaffin
Capryloyl Glycine
Cedrus Atlantica Bark Extract
Cetyl Lactate
Cinnamomum Zeylanicum Bark Extract
Cocamidopropyl PG-Dimonium Chloride Phosphate
Cyclopentasiloxane
Dehydroxanthan Gum
Denatonium Benzoate
Fragrance
Glycerin
Hamamelis Virginiana (Witch Hazel) Water
Laureth-7
Phenoxyethanol
Polyacrylamide
Polysorbate 20
Portulaca Oleracea Extract
PPG-2 Isoceteth-20 Acetate
Propylene Glycol
Sarcosine
t-Butyl Alcohol
Tetrasodium EDTA
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
346298salicylic acid 2 % Topical GelPSN1
346298salicylic acid 0.02 MG/MG Topical GelSCD1
346298salicylic acid 2 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-7782-012020-01-31C16284748780-19d75b9d0-24fa-f424-e053-dadaa90a57ceWell at Walgreens Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-7782-01Spot Acne Treatment21 g in 1 TUBEGEL211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-7782SPOT ACNE TREATMENT (SALICYLIC ACID) GEL [WALGREENS]1Legacy NDC, 1 package rows20180430_bebe2d42-09af-4ed3-b74a-394830bc32e4.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-77820363-7782-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
7f7e19da-a5d0-407c-a6b5-030248746e63bebe2d42-09af-4ed3-b74a-394830bc32e42018-04-30WarningsExact identifier
spl id: 7f7e19da-a5d0-407c-a6b5-030248746e63
spl set id: bebe2d42-09af-4ed3-b74a-394830bc32e4

Reported adverse events (FAERS/openFDA)#

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