FDA.reportPublic FDA data

NAS Toner

Manufacturer
BURT'S BEES, INC.
Effective date
2018-12-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:39:49

Label at a glance#

ProductNAS Toner
Active ingredientSALICYLIC ACID
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1.0%

OTC - PURPOSE SECTION

Acne Treatment

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings 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. In the rare case of an adverse reaction, discontinue use. If symptoms persist seek medical advice.

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 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 INGREDIENT SECTION

Inactive Ingredients: water, alcohol denat., glycerin, salix nigra (willow) bark extract, cymbopogon schoenanthus extract, hamamelis
virginiana (witch hazel) leaf extract, humulus lupulus (hops) extract, hydrastis canadensis (goldenseal) extract, fragrance, phenoxyethanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BURT'S BEES

natural

ACNE

SOLUTIONS

Salicylic Acid Acne

Treatment from Willow Bark

clarifying

TONER

Acne TonerAcne Toner

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
26052-03826052-038-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
HUMULUS LUPULUS WHOLE912A6Q1N4AIACT
SALICYLIC ACIDO414PZ4LPZACTIB
CYMBOPOGON SCHOENANTHUS TOP9SJI1LW39WIACT
GLYCERINPDC6A3C0OXIACT
SALIX NIGRA BARKQU52J3A5B3IACT
WATER059QF0KO0RIACT
HAMAMELIS VIRGINIANA TOPUDA30A2JJYIACT
GOLDENSEALZW3Z11D0JVIACT
ALCOHOL3K9958V90MIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
06ea4a82-eca9-6320-e063-6394a90ab9a07d784a5e-7b0a-03ca-e053-2a91aa0ac3662023-10-04WarningsExact identifier
spl set id: 7d784a5e-7b0a-03ca-e053-2a91aa0ac366

Reported adverse events (FAERS/openFDA)#

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