Alcohol pads by SHENZHEN BENLIJU BIO-TECH CO.,LTD ALCOHOL PADS patch

Alcohol pads by

Drug Labeling and Warnings

Alcohol pads by is a Otc medication manufactured, distributed, or labeled by SHENZHEN BENLIJU BIO-TECH CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

lsopropyl Alcohol

PURPOSE

disinfect

INDICATIONS & USAGE

For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes

WARNINGS

*For extemal use only.
*Flammable. keep away from fire or flame.
*Do not use " with electrocautery procedures " in the eyes. lf contact occurs, flush eyes with water.
*Stop use if irritation and redness develop. If condition persists consult your health care practioner.

DO NOT USE

Keep out of reach of children, lf swallowed, get medical help or contact a Poison Control Center rightaway.

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

For preparation of the skin prior to an injection and to decrease germs in minor cuts and scrapes.

STORAGE AND HANDLING

Store at room temperature.

INACTIVE INGREDIENT

Purified Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALCOHOL PADS 
alcohol pads patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84449-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	30 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84449-001-02	100 in 1 PATCH	06/14/2024
1	NDC: 84449-001-01	70 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)	06/14/2024

Labeler - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)

Registrant - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)

Establishment
Name	Address	ID/FEI	Business Operations
SHENZHEN BENLIJU BIO-TECH CO.,LTD		551073413	manufacture(84449-001)