AQUATO INTENSIVE CALMINGLOTION- adenosine lotion

Aquato Intensive CalmingLotion by

Drug Labeling and Warnings

Aquato Intensive CalmingLotion by is a Otc medication manufactured, distributed, or labeled by Natural Story Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

adenosne

INACTIVE INGREDIENT

WATER
GLYCERIN
ETHYLHEXYL STEARATE
1,2-HEXANEDIOL
CETEARYL ALCOHOL
POLYGLYCERYL-3 DISTEARATE
GLYCERYL STEARATE CITRATE
PHENYL TRIMETHICONE
WATER
DIPROPYLENE GLYCOL
GLYCERIN
LAMINARIA JAPONICA EXTRACT
ECLIPTA PROSTRATA LEAF EXTRACT
1,2-HEXANEDIOL
FRUCTOOLIGOSACCHARIDES
BETA-GLUCAN
HYDROGENATED LECITHIN
HYDROLYZED HYALURONIC ACID
METHYL TRIMETHICONE
PROPANEDIOL
WATER
GLYCERIN
1,2-HEXANEDIOL
BETA-GLUCAN
WATER
BUTYLENE GLYCOL
1,2-HEXANEDIOL
ULMUS DAVIDIANA ROOT EXTRACT
AMARANTHUS CAUDATUS SEED EXTRACT
GLYCERYL STEARATE
GLYCERIN
BUTYLENE GLYCOL
WATER
HYDROGENATED LECITHIN
FICUS CARICA (FIG) FRUIT EXTRACT
CENTELLA ASIATICA EXTRACT
1,2-HEXANEDIOL
CERAMIDE NP
SODIUM STEAROYL GLUTAMATE
ARGININE
CARBOMER
BETAINE
BEHENYL ALCOHOL
CETEARYL ALCOHOL
HYDROGENATED LECITHIN
GLYCERYL STEARATE SE
CHOLESTEROL
CERAMIDE NP
ETHYLHEXYLGLYCERIN
TOCOPHEROL
CARBOMER
WATER
1,2-HEXANEDIOL
GLYCOSAMINOGLYCANS
WATER
1,2-HEXANEDIOL
UNDARIA PINNATIFIDA EXTRACT
DISODIUM EDTA

PURPOSE

special skincare for dry and sensitive skin with abundant moisture and sea algae extract

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

apply proper amount to the skin

WARNINGS

Keep out of reach of children.

Store in a cool, dry place and avoid direct sunlight.

Do not inhale or drink it.

Discontinue use if skin allergy or discomfort occurs.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AQUATO INTENSIVE CALMINGLOTION 
adenosine lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80972-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S) (UNDARIA PINNATIFIDA - UNII:ICV1OK7M1S)	UNDARIA PINNATIFIDA	0.0005 g  in 100 mL
HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) (UNII: 997385V0VV) (HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) - UNII:997385V0VV)	HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW)	0.001 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: 80972-0002-1	160 mL in 1 TUBE; Type 0: Not a Combination Product	12/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/25/2020

Labeler - Natural Story Co.,Ltd. (557783679)

Registrant - Natural Story Co.,Ltd. (557783679)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Story Co.,Ltd.		557783679	manufacture(80972-0002) , label(80972-0002)