Natural Acne Solutions Clarifying Toner

Manufacturer
Burt's Bees, Inc.
Effective date
2010-08-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:33

Label at a glance#

ProductNatural Acne Solutions Clarifying Toner
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

Penetrates pores to control acne Helps prevent the development of new blemishes

Dosage and administration

After cleansing and/or exfoliating, moisten a cotton pad with toner and apply to face and neck using upward movements, avoiding the eye area.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1.0%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

  • Penetrates pores to control acne
  • Helps prevent the development of new blemishes

Warnings

WARNINGS SECTION

For external use only.

Using other topical acne medication at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

After cleansing and/or exfoliating, moisten a cotton pad with toner and apply to face and neck using upward movements, avoiding the eye area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aqua (water, eau), alcohol denat., glycerin, salix nigra (willow) bark extract, cymbopogon schoenanthus extract, equisetum hiemale extract, parfum (fragrance), hamamelis virginiana (witch hazel) leaf extract, humulus lupulus (hops) extract, hydrastis canadensis (goldenseal) extract, glucose, sodium chloride, glucose oxidase, lactoperoxidase

PDP Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottlePackage LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047362salicylic acid 1 % Topical SolutionPSN1
1047362salicylic acid 10 MG/ML Topical SolutionSCD1
1047362salicylic acid 1 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
26052-017-022019-10-21C16284748780-1956f9ecf-c564-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
26052-017-01Natural Acne Solutions Clarifying Toner175 mL in 1 BOTTLELIQUID1751
26052-017-02Natural Acne Solutions Clarifying Toner1 in 1 BOXLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
26052-017NATURAL ACNE SOLUTIONS CLARIFYING TONER (SALICYLIC ACID) LIQUID [BURT'S BEES, INC.]1Legacy NDC, 2 package rows20100816_f009d082-947f-455d-912f-c2c111001a30.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
26052-01726052-017-01, 26052-017-02

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB

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
fe5af802-5290-442f-a715-7b8c54fa2e38f009d082-947f-455d-912f-c2c111001a302010-08-16WarningsExact identifier
spl id: fe5af802-5290-442f-a715-7b8c54fa2e38
spl set id: f009d082-947f-455d-912f-c2c111001a30

Reported adverse events (FAERS/openFDA)#

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