PHOEBUSBIO 75% ALCOHOL HAND SANITIZER- alcohol hand sanitizer gel

PhoebusBio 75% Alcohol hand sanitizer by

Drug Labeling and Warnings

PhoebusBio 75% Alcohol hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Weifang Hongyang Pharmacy Co., Ltd., A03 Lab of BTS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

The product has a killing effect on Staphylococcus aureus, E. coli, Candida albicans, and Pseudomonas aeruginosa.

This product is suitable for sanitary hand disinfection and Skin disinfection.

Use

[Sanitary hand disinfection]: Evenly apply the product to the hand for 1-2 times, and stay for 1 min.

[Skin disinfection]: Evenly apply the product to the skin surface for 2 times, and stay for 3 minutes.

Warnings

1. External disinfectants should not be taken orally and should be kept out of reach of children.

2. Flammable, keep away from fire.

3. Use with caution to those who are allergic to alcohol.

4. Not suitable for disinfection of fat-soluble objects.

Do not use

• on children less than 2 months of age
• on open skin wounds
• for disinfection of fat-soluble objects

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.

Directions

[Sanitary hand disinfection]: Evenly apply the product to the hand for 1-2 times, and stay for 1 min.

[Skin disinfection]: Evenly apply the product to the skin surface for 2 times, and stay for 3 minutes.

Other information

Storage conditions: Protect from light, store in a cool, dry, ventilated place.

Inactive ingredients

Water, Carbomer.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

PHOEBUSBIO 75% ALCOHOL HAND SANITIZER 
alcohol hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72153-213
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	375 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	122 mL  in 500 mL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	3 mL  in 500 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72153-213-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/20/2020

Labeler - Weifang Hongyang Pharmacy Co., Ltd. (529650702)

Registrant - A03 Lab of BTS (548009541)

Establishment
Name	Address	ID/FEI	Business Operations
Weifang Hongyang Pharmacy Co., Ltd.		529650702	label(72153-213) , manufacture(72153-213)