ANTIBACTERIAL HAND SANITIZER- alcohol swab

Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Webb Business Promotions, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingridient

Ethyl Alcohol 75%

PURPOSE

Antiseptic

WHEN USING

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

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.

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.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

Water, Aloe essential oil

INDICATIONS & USAGE

Hand Sanitizer to help decrease bacteria on the skin

DOSAGE & ADMINISTRATION

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND SANITIZER 
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70445-417
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70445-417-01	1 mL in 1 POUCH; Type 0: Not a Combination Product	02/01/2021
2	NDC: 70445-417-02	10 mL in 1 POUCH; Type 0: Not a Combination Product	02/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/01/2021

Labeler - Webb Business Promotions, Inc (154445647)

Registrant - Webb Business Promotions, Inc (154445647)

Establishment
Name	Address	ID/FEI	Business Operations
Webb Business Promotions, Inc		154445647	relabel(70445-417) , repack(70445-417) , manufacture(70445-417) , label(70445-417)