ANZOON ANTIBACTERIAL MOUTH WASH- cetylpyridinium chloride liquid

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredient

Cetylpyridinium Chloride 0.027%

Purpose

Oral Antibacterial

Uses

Antigingivitis, Antiplaque, Anti-caries

Warnings

For external use only

When using this product

Avoided in: 1 Thyroid disorders 2. Pregnant/Breastfeeding

Used only upon advice by healthcare professional

Stop use and ask a doctor

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children

If swallowed, get medical help, or contact a Poison COntrol Center right away.

Directions

1.Pour the anzoon Gargle & Mouthwash into the cup 20 ml

2. Swish part of the solution briefly in mouth and s[it it out

3. Tilt head back, gargle for 30 seconds at the throat and spit it out

4. Repeated every two to four hours or as directed

Inactive ingredients

Water, sorbitol, Potassium Sorbate, Sodium Benzoate, Xylitol, Menthol,Pomegranate Extract

Other information

Store between 15-30 ºC(59-86°F)

Do not store above 100 °F(43°C)

Label

INGREDIENTS AND APPEARANCE

ANZOON ANTIBACTERIAL MOUTH WASH 
cetylpyridinium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87638-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3)	CETYLPYRIDINIUM CHLORIDE	0.027 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
MENTHOL (UNII: L7T10EIP3A)
POMEGRANATE (UNII: 56687D1Z4D)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
XYLITOL (UNII: VCQ006KQ1E)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87638-002-01	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026
2	NDC: 87638-002-02	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026
3	NDC: 87638-002-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026
4	NDC: 87638-002-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026
5	NDC: 87638-002-05	260 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026
6	NDC: 87638-002-06	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026
7	NDC: 87638-002-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026
8	NDC: 87638-002-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	04/28/2026

Labeler - Shandong AZC Biotechnology Co.,Ltd. (844599612)

Establishment
Name	Address	ID/FEI	Business Operations
Shandong AZC Biotechnology Co.,Ltd.		844599612	manufacture(87638-002)