BREATH MELLOW WATER LILY- cetylpyridinium chloride spray 
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Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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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

Image of bottle

BREATH MELLOW WATER LILY 
cetylpyridinium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72265-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.0085 g  in 17 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Alcohol (UNII: 3K9958V90M)  
Glycerin (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72265-102-0117 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/01/2021
Labeler - CURESCRIPT (694894509)
Registrant - CURESCRIPT (694894509)
Establishment
NameAddressID/FEIBusiness Operations
Biostech Co., Ltd.687294330manufacture(72265-102)

Revised: 2/2021
Document Id: 39d6e116-bb51-4dc4-8cdb-543c90d7f63c
Set id: d37ae939-a0e3-47b7-8cd8-bce91b9a28b7
Version: 2
Effective Time: 20210223
 
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