FLAWLESS HAND SANITIZER- propolis extract spray

FLAWLESS HAND SANITIZER by

Drug Labeling and Warnings

FLAWLESS HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by NBIO CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Propolis Extract 0.5%

INACTIVE INGREDIENTS

Water, Sodium Silicate

PURPOSE

Sanitizer

WARNINGS

■ For external use only.
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When using this product
■ Do not use in or near the eyes. In case of contact, rinse eyes thoroughly
with water.
■ Avoid contact with broken skin.
■ Do not inhale or ingest.
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Stop use and ask a doctor
■ If irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

■ If swallowed, get medical help or contact a Poison Control Center right away

Uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.
■ For use when soap and water are not available.

Directions

■ Please spray it at a distance of 10~20cm so that your hands are enough covered. Rub hands together until dry.
■ Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

■ Store between 41~86℉(Between 5~30℃)
■ Avoid freezing and excessive heat above 104℉(40℃) and direct sunlight.

QUESTIONS

■ www.nbio.kr / 82-31-432-5670

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FLAWLESS HAND SANITIZER 
propolis extract spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77560-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF)	PROPOLIS WAX	1.25 g  in 250 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium Silicate (UNII: IJF18F77L3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77560-010-01	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2020

Labeler - NBIO CO., LTD. (687218375)

Registrant - NBIO CO., LTD. (687218375)

Establishment
Name	Address	ID/FEI	Business Operations
NBIO CO., LTD.		687218375	manufacture(77560-010)