BREATH MELLOW WATER LILY- cetylpyridinium chloride spray

Breath mellow Water Lily by

Drug Labeling and Warnings

Breath mellow Water Lily by is a Otc medication manufactured, distributed, or labeled by CURESCRIPT, Biostech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

CETYLPYRIDINIUM CHLORIDE 0.05%

INACTIVE INGREDIENTS

Water, Ethanol, Glycerin , Flavor , Xylitol , L-Menthol, Polysorbate 80 , PEG-40 Hydrogenated Castor Oil , Poloxamer 407 , Saccharin Sodium Dihydrate , Enzymatically Modified Stevia Glucosyl Stevia , Cetyl Pyridinium Chloride , Eucalyptus oil , Citric acid, Sodium Citrate, Peony root Extract, Syzygium aromaticum extract , Betula Platyphylla Japonica Bark Extract , Peppermint oil , Green tea Extract , Scutellaria Baicalensis Extract , Nasturtium Officinale Extract , Rubus Idaeus (Raspberry) Fruit Extract , Petroselinum Sativum (Parsley) Extract, Gardenia Jasminoides Fruit Extract

PURPOSE

Oral Antiseptic

WARNINGS

■ Do not use if you are allergic to any of the ingredients

Stop use and ask a dentist if ■Swelling, rash or fever develops. ■ Irritation, pain or redness persists or worsens.

Keep out of the reach of children

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

■ Helps control bad breath
■ aids in the removal or debris, dental plaque and control bacteria.

Directions

■ Spray directly into mouth, onto the tongue and spread thoroughly inside the mouth.
■ Children 12 years and under Not for us unless directed by a healthcare professional

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BREATH MELLOW WATER LILY 
cetylpyridinium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72265-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3)	CETYLPYRIDINIUM CHLORIDE	0.0085 g  in 17 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Alcohol (UNII: 3K9958V90M)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72265-102-01	17 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/01/2021

Labeler - CURESCRIPT (694894509)

Registrant - CURESCRIPT (694894509)

Establishment
Name	Address	ID/FEI	Business Operations
Biostech Co., Ltd.		687294330	manufacture(72265-102)