ANTISEPTIC- alcohol cloth

Antiseptic by

Drug Labeling and Warnings

Antiseptic by is a Otc medication manufactured, distributed, or labeled by Safetec of America, Inc., Safetec of America, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Ethyl Alcohol 66.5%

Purpose

Antiseptic

Uses

• Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water

Warnings

For external use only

Flammable: keep away from fire or flame

Do not use in the eyes. If this happens, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours

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

Directions

• tear open packet, remove towelette
• unfold and use as a washcloth
• supervise children under 6 years of age

Inactive ingredients

aloe vera, fragrance, purified water, triethanolamine

Principal Display Panel - Safetec Antiseptic Towelette Carton Label

NDC: 61010-2017-1

Safetec

Antiseptic
Towelette

For Professional and Hospital Use

Contents: 100 single-use, premoistened towelettes

Reorder No. 38400

Principal Display Panel - Safetec Antiseptic Towelette Packet Label

Safetec

Antiseptic
Towelette

For Professional and Hospital Use

Contents: 1 single-use, premoistened towelette

Manufactured by SAFETEC OF AMERICA, Inc.

Buffalo, NY 14215 800-456-7077 www.safetec.com

INGREDIENTS AND APPEARANCE

ANTISEPTIC 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61010-2017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M)	alcohol	665 mL  in 1 L

Inactive Ingredients
Ingredient Name	Strength
aloe vera leaf (UNII: ZY81Z83H0X)
water (UNII: 059QF0KO0R)
trolamine (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61010-2017-0	.0019 L in 1 PACKET; Type 0: Not a Combination Product	05/01/2017
2	NDC: 61010-2017-1	100 in 1 BOX	05/01/2017
2		.0019 L in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2017

Labeler - Safetec of America, Inc. (874965262)

Establishment
Name	Address	ID/FEI	Business Operations
Safetec of America, Inc		874965262	MANUFACTURE(61010-2017)