FDA.reportPublic FDA data

BERRY MEDLEY THROAT DROPS

Manufacturer
Ricola USA Inc. | Ricola Ag
Effective date
2024-12-10
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 00:41:39

Label at a glance#

ProductBERRY MEDLEY THROAT DROPS
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 6 years and older:  dissolve 2 drops (one at a time) slowly in the mouth.  Do not bite or chew.  Repeat every 2 hours as needed or as directed by a doctor children under 6 years: ask a doctor

Storage and handling

protect from heat and moisture

Label contents#

Full prescribing information#

Drug Facts

OTC - PURPOSE SECTION

Purpose

Oral anesthetic

Active Ingredient (in each drop)

OTC - ACTIVE INGREDIENT SECTION

Menthol, 1.7 mg

Uses

INDICATIONS & USAGE SECTION

temporarily relieves occasional minor irritation and pain associated with:

  • sore mouth
  • sore throat

Warnings

WARNINGS SECTION

Do not use

  • in children under 6 years of age unless directed by a doctor.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

  • sore throat is severe, persists for more than 2 days, or is accompanied by fever, headache, rash, nausea or vomiting.
  • sore mouth symptoms do not improve in 7 days.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 6 years and older:  dissolve 2 drops (one at a time) slowly in the mouth.  Do not bite or chew.  Repeat every 2 hours as needed or as directed by a doctor
  • children under 6 years: ask a doctor

Other Information

STORAGE AND HANDLING SECTION

protect from heat and moisture

Inactive Ingredients

INACTIVE INGREDIENT SECTION

bilberry juice concentrate, black currant juice concentrate, citric acid, extract of Ricola herb mixture (lemon balm, peppermint, thyme, hyssop, sage, elder, linden, mallow, horehound, wild thyme), glucose syrup, natural color, natural flavors, peppermint oil, raspberry juice concentrate, sugar

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Berry Medley.jpgImage of Berry Medley.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
665080menthol 1.7 MG Oral LozengePSN7
665080menthol 1.7 MG Oral LozengeSCD7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63667-436-10BERRY MEDLEY THROAT DROPS10 in 1 BAGLOZENGE107
63667-436-19BERRY MEDLEY THROAT DROPS19 in 1 BAGLOZENGE197
63667-436-45BERRY MEDLEY THROAT DROPS45 in 1 BAGLOZENGE457

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63667-436BERRY MEDLEY THROAT DROPS (MENTHOL) LOZENGE [RICOLA USA INC.]7Current NDC, Legacy NDC, 3 package rows20241211_9bfd2ea7-745b-47f8-bd8a-9dbeeaad8b95.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63667-43663667-436-45, 63667-436-19, 63667-436-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SUCROSEC151H8M554IACT

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
BERRY MEDLEY THROAT DROPSMENTHOLRicola USA Inc.9bfd2ea7-745b-47f8-bd8a-9dbeeaad8b952024-12-10WarningsExact identifier
ndc (package): 63667-436-10
ndc (package): 63667-436-19
ndc (package): 63667-436-45
ndc (product): 63667-436
ndc11 (package): 63667043645
ndc11 (package): 63667043610
ndc11 (package): 63667043619
spl id: 61ac405a-6276-4f82-be35-c19ef8290359
spl set id: 9bfd2ea7-745b-47f8-bd8a-9dbeeaad8b95

Reported adverse events (FAERS/openFDA)#

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