NATURAL CHERRY HONEY HERB THROAT DROPS- menthol lozenge

Natural Cherry Honey Herb Throat Drops by

Drug Labeling and Warnings

Natural Cherry Honey Herb Throat Drops by is a Otc medication manufactured, distributed, or labeled by Ricola USA Inc., Ricola Ag. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Purpose

Oral anesthetic

Active Ingredient (in each drop)

Menthol, 2.1 mg

Uses

temporarily relieves occasional minor irritation and pain associated with:

• sore mouth
• sore throat

Warnings

Do not use

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

Stop use and ask a doctor if

• 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

Keep out of reach of children.

Directions

• 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

protect from heat and moisture

Inactive Ingredients

extract of a Ricola herb mixture (elder, horehound, hyssop, lemon balm, linden flowers, mallow, peppermint, sage, thyme, wild thyme), honey, malic acid, natural cherry concentrate, natural color, natural flavors, starch syrup, sugar

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATURAL CHERRY HONEY HERB THROAT DROPS 
menthol lozenge

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63667-517
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2.1 mg

Inactive Ingredients
Ingredient Name	Strength
MALIC ACID (UNII: 817L1N4CKP)
HONEY (UNII: Y9H1V576FH)
CHERRY (UNII: BUC5I9595W)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	red	Score	no score
Shape	RECTANGLE	Size	19mm
Flavor	CHERRY (CHERRY HONEY)	Imprint Code	R
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63667-517-09	9 in 1 PACKAGE; Type 0: Not a Combination Product	01/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	01/01/2022

Labeler - Ricola USA Inc. (177265261)

Establishment
Name	Address	ID/FEI	Business Operations
Ricola Ag		480227248	manufacture(63667-517)