Cherry Throat Drops

Manufacturer: Ricola Ag
Effective date: 2024-12-05
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:40:34

Label at a glance#

ProductCherry 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, 1.4 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

cherry concentrate, colors (cerrot and hibiscus concentrate), extract of Ricola herb mixture (elder, horehound, hyssop, lemon balm, linden flowers, mallow, peppermint, sage, thyme, wild thyme), flavors (bitter almond and cherry), glucose syrup, malic acid, sugar

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Ricola Cherry Bag 19.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2634994	menthol 1.4 MG Oral Lozenge	PSN	3
2634994	menthol 1.4 MG Oral Lozenge	SCD	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54305-910-19	Cherry Throat Drops	19 in 1 BAG	LOZENGE	19		3
54305-910-45	Cherry Throat Drops	45 in 1 BAG	LOZENGE	45		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54305-910	CHERRY THROAT DROPS (MENTHOL) LOZENGE [RICOLA AG]	3	Current NDC, 2 package rows	20241207_73d767e2-bb80-4eff-8420-500c2a4067aa.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Cherry Throat Drops
MENTHOL
MALIC ACID
CHERRY
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54305-910	54305-910-19, 54305-910-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
MALIC ACID	817L1N4CKP	IACT
CHERRY	BUC5I9595W	IACT
SUCROSE	C151H8M554	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cherry Throat Drops	MENTHOL	Ricola Ag	73d767e2-bb80-4eff-8420-500c2a4067aa	2024-12-05	Warnings	Exact identifier ndc (package): 54305-910-45 ndc (package): 54305-910-19 ndc (product): 54305-910 ndc11 (package): 54305091045 ndc11 (package): 54305091019 spl id: b155a548-8176-4acc-a0f6-384d18f4d9b3 spl set id: 73d767e2-bb80-4eff-8420-500c2a4067aa

Reported adverse events (FAERS/openFDA)#

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