La GRACE Aqua Perfect Hand Sanitizer gel by WINNOVA Co., Ltd. Drug Facts

La GRACE Aqua Perfect Hand Sanitizer gel by

Drug Labeling and Warnings

La GRACE Aqua Perfect Hand Sanitizer gel by is a Otc medication manufactured, distributed, or labeled by WINNOVA Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LA GRACE AQUA PERFECT HAND SANITIZER GEL- alcohol gel 
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.

■ Flammable. Keep away from fire or flame.

■ 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

LA GRACE AQUA PERFECT HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76934-0003
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)
CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
CARBOMER 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
SAGE (UNII: 065C5D077J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76934-0003-1	100 mL in 1 TUBE; Type 0: Not a Combination Product	06/13/2020	08/04/2022
2	NDC: 76934-0003-2	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020	08/04/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/13/2020	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(76934-0003)

Revised: 8/2022

Document Id: e56300e6-0a6a-8d80-e053-2a95a90a82e3

34390-5

Set id: a7f7afa7-c990-3aaf-e053-2a95a90a45eb

Version: 2

Effective Time: 20220803