ANTISEPTIC- antiseptic spray spray

Antiseptic by

Drug Labeling and Warnings

Antiseptic by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

First Aid Antiseptic

Use(s)

First aid to help prevent infection in minor cuts, scrapes, and burns

Warnings

For External Use Only

Flammable. Keep away from fire or flame.

Do not use

Near eyes or mucous membranes Over large areas of the body More than 1 week unless directed by a doctor

Ask a doctor before use if you have

Deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

Irritation and redness develop Condition persists or gets worse

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Clean the affected area and spray 1 to 3 times daily

May be covered with a sterile bandage

If bandaged, let dry first

Children under 12 years of age: Consult a doctor before use

Other Information

Store at 20º-25ºC (68°-77ºF)

Avoid excessive heat

Inactive Ingredients

Ethyl Alcohol, Purified Water

Questions?

1-888-Dynarex Monday - Friday, 9AM - 5PM EST

Label

1167 Label

INGREDIENTS AND APPEARANCE

ANTISEPTIC 
antiseptic spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL 95% (UNII: 7528N5H79B)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-012-03	24 in 1 CASE	02/29/2024
1	NDC: 67777-012-04	59.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	02/29/2024

Labeler - Dynarex Corporation (008124539)