FDA.reportPublic FDA data

NATURAL THROAT DROPS HONEY

Manufacturer
BURT'S BEES, INC.
Effective date
2021-11-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:29:28

Label at a glance#

ProductNATURAL THROAT DROPS HONEY
Active ingredientMENTHOL
Label structure9 sections

Indications and uses

TEMPORARILY RELIEVES OCCASIONAL MINOR IRRITATION AND PAIN ASSOCIATED WITH: SORE MOUTH SORE THROAT

Dosage and administration

ADULTS AND CHILDREN 5 YEARS AND OVER: DISSOLVE 2 DROPS (ONE AT A TIME) SLOWLY IN MOUTH. REPEAT EVERY 2 HOURS AS NEEDED. CHILDREN UNDER 5: CONSULT A DOCTOR.

Storage and handling

STORE IN A COOL, DRY PLACE

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

MENTHOL 2.0 MG

PURPOSE

OTC - PURPOSE SECTION

ORAL PAIN RELIEVER

USES

INDICATIONS & USAGE SECTION

TEMPORARILY RELIEVES OCCASIONAL MINOR IRRITATION AND PAIN ASSOCIATED WITH:

SORE MOUTH

SORE THROAT

WARNINGS

WARNINGS SECTION

DO NOT EXCEED RECOMMENDED DOSAGE

STOP USE AND ASK A DOCTOR IF:

OTC - STOP USE SECTION

SORE THROAT IS SEVERE, PERSISTS FOR MORE THAN 2 DAYS, IS ACCOMPANIED OR FOLLOWED BY FEVER, HEADACHE, RASH, SWELLING, NAUSEA, OR VOMITING.

SORE MOUTH SYMPTOMS DO NOT IMPROVE IN 7 DAYS OR IF IRRITATION, PAIN OR REDNESS PERSISTS OR WORSENS.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

ADULTS AND CHILDREN 5 YEARS AND OVER: DISSOLVE 2 DROPS (ONE AT A TIME) SLOWLY IN MOUTH. REPEAT EVERY 2 HOURS AS NEEDED.

CHILDREN UNDER 5: CONSULT A DOCTOR.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

STORE IN A COOL, DRY PLACE

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

HONEY, SUCROSE, MALTODEXTRIN, ORYZA SATIVA (RICE) EXTRACT, WATER, FLAVOR, EUCALYPTUS GLOBULUS LEAF OIL

QUESTIONS?

OTC - QUESTIONS SECTION

CALL 800-849-7112

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BURT'S BEES

NATURAL THROAT DROPS

HONEY

WITH MENTHOL AND EUCALYPTUS

20 DROPS

HONEY THROAT DROPSHONEY THROAT DROPS

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
26052-02326052-023-01, 26052-023-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
ORYZA SATIVA WHOLE84IVV0906ZIACT
WATER059QF0KO0RIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
HONEYY9H1V576FHIACT
MALTODEXTRIN7CVR7L4A2DIACT
MENTHOLL7T10EIP3AACTIB

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
06f8876b-9275-b966-e063-6394a90a820b3168090a-ad36-103f-e054-00144ff8d46c2023-10-05WarningsExact identifier
spl set id: 3168090a-ad36-103f-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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