FDA.reportPublic FDA data

NAS Targeted Spot Treatment

Manufacturer
Burt's Bees
Effective date
2020-12-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:02:40

Label at a glance#

ProductNAS Targeted Spot Treatment
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

Penetrates pores to control acne

Dosage and administration

Apply to face in the morning and evening after cleansing.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.75%

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

  • Penetrates pores to control acne

Warnings

WARNINGS SECTION

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

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to face in the morning and evening after cleansing.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: alcohol denat., citrus medica limonum (lemon) peel oil, water, achillea millefolium extract, borago officinalis extract, calendula officinalis flower extract, carum petroselinum (parsley) extract, foeniculum vulgare (fennel) oil, salix nigra (willow) bark extract, melaleuca alternifolia (tea tree) leaf oil, eucalyptus globulus leaf oil, juniperus communis fruit oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BURT'S BEES

natural

ACNE SOLUTIONS

Salicylic Acid Acne

Treatment from Willow Bark

targeted

SPOT TREATMENT

100% Natural

0.26 fl oz / 7.5 ml

pdppdp

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
26052-01126052-011-01, 26052-011-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
SALICYLIC ACIDO414PZ4LPZACTIB
FENNEL OIL59AAO5F6HTIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
LEMON OILI9GRO824LLIACT
BORAGO OFFICINALIS SEED2GXJ790US0IACT
PARSLEY OILIXK9N7RJ7JIACT
SALIX NIGRA BARKQU52J3A5B3IACT
TEA TREE OILVIF565UC2GIACT
JUNIPER BERRY OILSZH16H44UYIACT
ACHILLEA MILLEFOLIUM2FXJ6SW4PKIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

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
06ea43ca-6159-e9c8-e063-6294a90ae1ed3102f14b-be7c-116f-e054-00144ff88e882023-10-04WarningsExact identifier
spl set id: 3102f14b-be7c-116f-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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