Label: AQUATO INTENSIVE CALMINGLOTION- adenosine lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 80972-0002-1 - Packager: Natural Story Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated December 25, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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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
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AQUATO INTENSIVE CALMINGLOTION
adenosine lotionProduct 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)