APOLLO ANTISEPTIC HAND SANITIZER- ethyl alcohol gel

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 75% 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  Aloe Barbadensis leaf Extract, Acrylates/ C10-30 alkyl Acrylate Crosspolymer, Triethanolaminel Ethylenediamine, 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

Moisturizing

Topical 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 gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77279-275
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)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
EDETOL (UNII: Q4R969U9FR)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77279-275-24	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
2	NDC: 77279-275-26	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/30/2020

Labeler - Seber Design Group, Llc (078349592)