RICOLA MAX NASAL CARE COOL MENTHOL

Manufacturer: Ricola USA Inc. | Ricola Ag
Effective date: 2024-12-10
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:41:40

Label at a glance#

ProductRICOLA MAX NASAL CARE COOL MENTHOL

Active ingredientMENTHOL

Label structure8 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 1 drop slowly in the mouth. Repeat every 2 hours as needed or as directed by a doctor. children under 6 years: ask a doctor do not bite or chew

Storage and handling

Store in a dry place

Label contents#

Full prescribing information#

Drug Facts

OTC - PURPOSE SECTION

Purpose

Oral anesthetic

Active Ingredient (in each drop)

OTC - ACTIVE INGREDIENT SECTION

Menthol, 15.3 mg

Uses

INDICATIONS & USAGE SECTION

temporarily relieves occasional minor irritation and pain associated with:

sore mouth
sore throat

Warnings

WARNINGS SECTION

Sore throat warnings:

if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 6 years and older: dissolve 1 drop slowly in the mouth. Repeat every 2 hours as needed or as directed by a doctor.
children under 6 years: ask a doctor
do not bite or chew

Other Information

STORAGE AND HANDLING SECTION

Store in a dry place

Inactive Ingredients

INACTIVE INGREDIENT SECTION

extract of lemon balm and the Ricola herb mixture (elder, horehound, hyssop, lemon balm, linden flowers, mallow, peppermint, sage, thyme, wild thyme), colors (carrot, spirulina), flavors (lemon-thyme, peppermint), starch syrup, sugar

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Cropped 9014328_US_NEO_US-MAX_Nasal Cool Menthol_34ct_Film_low - Flat File.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2599614	menthol 15.3 MG Oral Lozenge	PSN	3
2599616	Ricola 15.3 MG Oral Lozenge	PSN	3
2599616	menthol 15.3 MG Oral Lozenge [Ricola]	SBD	3
2599614	menthol 15.3 MG Oral Lozenge	SCD	3
2599616	Ricola 15.3 MG Oral Lozenge	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63667-206-34	RICOLA MAX NASAL CARE COOL MENTHOL	34 in 1 BAG	LOZENGE	34		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63667-206	RICOLA MAX NASAL CARE COOL MENTHOL (MENTHOL) LOZENGE [RICOLA USA INC.]	3	Current NDC, Legacy NDC, 1 package rows	20241211_a2e189a2-65ae-48a9-99ad-8795334082df.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

RICOLA MAX NASAL CARE COOL MENTHOL
MENTHOL
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63667-206	63667-206-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
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
RICOLA MAX NASAL CARE COOL MENTHOL	MENTHOL	Ricola USA Inc.	a2e189a2-65ae-48a9-99ad-8795334082df	2024-12-10	Warnings	Exact identifier ndc (package): 63667-206-34 ndc (product): 63667-206 ndc11 (package): 63667020634 spl id: 95faae2a-ce4d-4fc4-a844-0a246cc85027 spl set id: a2e189a2-65ae-48a9-99ad-8795334082df

Reported adverse events (FAERS/openFDA)#

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