LaGRACE Aqua Perfect SanitizerSpray by WINNOVA Co., Ltd. Drug Facts

LaGRACE Aqua Perfect SanitizerSpray by

Drug Labeling and Warnings

LaGRACE Aqua Perfect SanitizerSpray by is a Otc medication manufactured, distributed, or labeled by WINNOVA Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LAGRACE AQUA PERFECT SANITIZERSPRAY- alcohol liquid 
WINNOVA Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

alcohol

Water
Butylene Glycol
Carbomer
Aminomethyl Propanol
Alcohol
Propylene Glycol
Eucalyptus Globulus Leaf Extract
Salvia Officinalis (Sage) Leaf Extract
Citrus Limon (Lemon) Fruit Extract
Camellia Sinensis Leaf Extract
Fragrance

Sterilization of hands and skin

KEEP OUT OF REACH OF THE CHILDREN

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

for external use only

label

LAGRACE AQUA PERFECT SANITIZERSPRAY 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76934-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
WATER (UNII: 059QF0KO0R)  
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76934-0002-150 mL in 1 TUBE; Type 0: Not a Combination Product06/06/202008/04/2022
2NDC: 76934-0002-2100 mL in 1 TUBE; Type 0: Not a Combination Product06/06/202008/04/2022
3NDC: 76934-0002-3500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/06/202008/04/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/06/202008/04/2022
Labeler - WINNOVA Co., Ltd. (689348571)
Registrant - WINNOVA Co., Ltd. (689348571)
Establishment
NameAddressID/FEIBusiness Operations
WINNOVA Co., Ltd.689348571manufacture(76934-0002)

Revised: 8/2022
 

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