APOLLO ANTISEPTIC HAND SANITIZER- ethyl alcohol solution

apollo ANTISEPTIC HAND SANITIZER by

Drug Labeling and Warnings

apollo ANTISEPTIC HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Seber Design Group, Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Ethyl alcohol 80% v/v

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses  hand sanitizer to decrease bacteria on the skin recommended for repeated use  for use when soap and water are not available

WARNINGS

Warnings

Flammable, keep away from fire/flame

For external use only

Do not use  in children less than 2 months of age  on open skin wounds

When using this product   do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if  irritation and redness develop condition persists for more than 72 hours

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

DOSAGE & ADMINISTRATION

Directions   wet hands thoroughly with product and allow to dry without wiping  supervise children under 6 years of age when using this product to avoid swallowing

STORAGE AND HANDLING

Other information   store between 15-30°C (59-86°F)  avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT

Inactive ingredients glycerin, hydrogen peroxide, water

QUESTIONS

Questions or comments?   +1-877-584-1434

You may also report serious side effects to this phone number.

Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Topical Solution

Non-sterile Solution

Distributed by: Seber Design Group, LLC,

964 E.Badillo St, #501, Covina, CA 91724

COUNTRY OF ORIGIN: CHINA

Packaging

INGREDIENTS AND APPEARANCE

APOLLO ANTISEPTIC HAND SANITIZER 
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77279-184
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77279-184-84	237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/22/2020

Labeler - Seber Design Group, Llc (078349592)