HAND SANITIZER WIPES cloth

Hand Sanitizer Wipes by

Drug Labeling and Warnings

Hand Sanitizer Wipes by is a Otc medication manufactured, distributed, or labeled by LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

Hand Sanitizer to help decrease bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For External Use Only.

When using this product Keep out of eyes. In case of contact with eyes,rinse with water.

Stop use and ask doctor if irritation and redness develops and persists.

Keep out of reach of children If swallowed, get medical help promptly and contact Poison Control.

WHEN USING

When using this product Keep out of eyes. In case of contact with eyes,rinse with water.

STOP USE

Stop use and ask doctor if irritation and redness develops and persists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children If swallowed, get medical help promptly and contact Poison Control.

Directions

• Remove wipe from pouch, thoroughly wash hands and arms with wipe and discard wipe when finished. Do not flush wipe.
• Children under 6 years should be supervised when using this product.

Other Infomation

Tightly replace resealable label on pouch to keep wipes from loosing moisture.

Inactive Ingredients

Water, Aloe essential oil

PRINCIPAL DISPLAY PANEL

Hand Sanitizer Wipes

1 count

NDC: 75269-011-01

Hand Sanitizer Wipes

10 count

NDC: 75269-011-02

INGREDIENTS AND APPEARANCE

HAND SANITIZER WIPES 
hand sanitizer wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75269-011
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 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75269-011-01	1 in 1 POUCH	12/13/2020
1		0.004 mL in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 75269-011-02	10 in 1 POUCH	12/13/2020
2		0.004 mL in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/13/2020

Labeler - LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD. (560972943)

Registrant - LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD. (560972943)

Establishment
Name	Address	ID/FEI	Business Operations
LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD.		560972943	manufacture(75269-011)