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

LaGRACE Aqua Perfect Hand SanitizerSpray by

Drug Labeling and Warnings

LaGRACE Aqua Perfect Hand 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 HAND 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
Propylene Glycol
Eucalyptus Globulus Leaf Extract
Salvia Officinalis (Sage) Leaf Extract
Citrus Limon (Lemon) Fruit Extract
Camellia Sinensis Leaf Extract
Fragrance

limonene

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

LAGRACE AQUA PERFECT HAND SANITIZERSPRAY 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76934-0005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SAGE OIL (UNII: U27K0H1H2O)
WATER (UNII: 059QF0KO0R)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76934-0005-1	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020	08/04/2022
2	NDC: 76934-0005-2	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020	08/04/2022
3	NDC: 76934-0005-3	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2020	08/04/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/06/2020	08/04/2022

Labeler - WINNOVA Co., Ltd. (689348571)

Registrant - WINNOVA Co., Ltd. (689348571)

Establishment
Name	Address	ID/FEI	Business Operations
WINNOVA Co., Ltd.		689348571	manufacture(76934-0005)

Revised: 8/2022

Document Id: e562da92-3a29-3e6d-e053-2995a90a8dca

34390-5

Set id: b0f25210-5a55-a499-e053-2995a90abfc6

Version: 2

Effective Time: 20220803