BLUE UNITY ALCOHOL WIPES- alcohol wipes cloth

Blue Unity Alcohol Wipes by

Drug Labeling and Warnings

Blue Unity Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Shandong Oushile Biotechnology Co.Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Ethyl Alcohol   Antiseptic

Use

Helps reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age.
• on open skin wounds.

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.

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

Directions

• Open the package and wipe skin until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

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

Manufactured by Shandong Oushile Biotechnology Co.Ltd

Made in China

Distributed by Rixi Group USA, Inc
8966 Mason Ave, Chatsworth, CA 91311
Phone: (818)341-6600
gary@rixiglobal.net

Inactive ingredients

CETYLPYRIDINIUM CHLORIDE, WATER

Package Label - Principal Display Panel

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BLUE UNITY ALCOHOL WIPES 
alcohol wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78781-408
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
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78781-408-01	175 in 1 PACKAGE; Type 0: Not a Combination Product	08/04/2020
2	NDC: 78781-408-04	50 in 1 PACKAGE; Type 0: Not a Combination Product	08/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/04/2020

Labeler - Shandong Oushile Biotechnology Co.Ltd (554531936)

Establishment
Name	Address	ID/FEI	Business Operations
Shandong Oushile Biotechnology Co.Ltd		554531936	manufacture(78781-408)