UNIFRESH ALL CLEAN ALCOHOL- alcohol wipes cloth

Unifresh All Clean alcohol by

Drug Labeling and Warnings

Unifresh All Clean alcohol by is a Otc medication manufactured, distributed, or labeled by TAISUN VIETNAM CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 75%

INACTIVE INGREDIENT

Water, Polyhexamethylenebiguanide hydrochloride, Diglycerin, PEG-40 hydrogenated castor oil, Aloe-vera extract, Fragrance

PURPOSE

Antiseptic

INDICATIONS & USAGE

Used for antibacterial hand skin, prevent bacteria.

WARNINGS

For external use only. Flammable. Keep away from fire.

DO NOT USE

Keep away from fire.
Do not wipe your eyes.
Do not throw into the toilet (not soluble in water).

WHEN USING

Please wait until the alcohol has completely evaporated after wiping.
Before use, check whether the packaging is intact. Do not use if it is damaged.

STOP USE

Stop use and ask a doctor for those with alcohol allergy or sensitive skin.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

STORAGE AND HANDLING

Store between 15-30°C (59-86°F).
Avoid freezing and excessive heat above 40°C (104°F).

DOSAGE & ADMINISTRATION

Use it as needed, after following the usage instructions. For external use only

PRINCIPAL DISPLAY PANEL

Unifresh All Clean Hand Sanitizer Wipes_60pcs

Unifresh All Clean Hand Sanitizer Wipes_20pcs

INGREDIENTS AND APPEARANCE

UNIFRESH ALL CLEAN ALCOHOL 
alcohol wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80493-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100

Inactive Ingredients
Ingredient Name	Strength
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)
DIGLYCERIN (UNII: 3YC120743U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80493-102-01	60 in 1 POUCH; Type 0: Not a Combination Product	09/03/2020
2	NDC: 80493-102-02	20 in 1 POUCH; Type 0: Not a Combination Product	10/19/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/03/2020

Labeler - TAISUN VIETNAM CO.,LTD (555278816)

Registrant - TAISUN VIETNAM CO.,LTD (555278816)

Establishment
Name	Address	ID/FEI	Business Operations
TAISUN VIETNAM CO.,LTD		555278816	manufacture(80493-102)