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

Ethyl alcohol 75% v/v

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

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 aqua, acrylates/c10-30 alkyl acrylate cross polymer, glycerin, tocopherol.

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: 77279-375
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
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77279-375-20	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
2	NDC: 77279-375-21	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
3	NDC: 77279-375-22	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
4	NDC: 77279-375-23	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
5	NDC: 77279-375-24	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
6	NDC: 77279-375-28	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - Seber Design Group, Llc (078349592)