COOL SENSE- propolis wax liquid

COOL SENSE by

Drug Labeling and Warnings

COOL SENSE by is a Otc medication manufactured, distributed, or labeled by Bncare Agriculture Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Propolis extract (total flavonoid 5%)

PURPOSE

Can help the antimicrobial action in the mouth

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

3 times a day, spray 0.5ml (approx. 2 times) once orally

WARNINGS

1. Those who are allergic to propolis should be careful about their intake, and those who have a specific or allergy should check their ingredients.
2. If you experience any of the symptoms, please stop intake, consult a specialist or contact the customer service.
3. Due to the nature of the raw materials, sediment may occur occasionally, but the quality is not abnormal.
4. Check the expiration date before ingesting and follow the intake and intake method.
5. Take care that the spray nozzle does not come in direct contact with your mouth and after spraying, clean and store the spray.

INACTIVE INGREDIENT

water, gamma-cyclodextrin, xylitol, anhydrous dextrose, glucosyl steviol, citric acid monohydrate, codonopsis pilosula whole (concentrate), pear (concentrate) juice, chitosan, turmeric, artificial flavor

DOSAGE & ADMINISTRATION

For dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

COOL SENSE 
propolis wax liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73706-0001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF)	PROPOLIS WAX	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73706-0001-2	2 in 1 CARTON	03/17/2020
1	NDC: 73706-0001-1	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 73706-0001-3	2 in 1 BLISTER PACK	03/17/2020
2	NDC: 73706-0001-1	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/17/2020

Labeler - Bncare Agriculture Co., Ltd. (688206563)

Registrant - Bncare Agriculture Co., Ltd. (688206563)

Establishment
Name	Address	ID/FEI	Business Operations
Bncare Agriculture Co., Ltd.		688206563	manufacture(73706-0001)