FIRST AID ANTISEPTIC- benzalkonium 0.13%, lidocaine hcl 2.5% spray

First Aid Antiseptic by

Drug Labeling and Warnings

First Aid Antiseptic by is a Otc medication manufactured, distributed, or labeled by Meijer, Product Quest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients                   Purpose

Benzalkonium 0.13%                First Aid Antiseptic

Lidocaine HCl 2.5%                 Pain Relieving Spray

Uses

First aid to help prevent bacterial contamination or skin infection, and for temporary relief of pain and itching associated with minor: cuts, scrapes, burns, sunburn, skin irritations

Warnings

​ ​For external use only

​Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

When using this product​

• do not use in or near the eyes
• do not apply over large area of the body or in large quantities
• do not apply over raw surfaces or blistered areas

​Stop use and ask a doctor if

• condition worsens
• symptoms persist for more than 7 days, or clear up and occur again within a few days

​Keep out of reach of children

​If swallowed get medical help or contact a Poison Control Center right away

Directions

Adults and children 2 years and older: clean the affected area. Apply small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first) Children Under 2 years: Consult a physician.

Other information

Avoid excessive heat

Inactive ingredients

Diazolidinyl Urea, Disodium EDTA, Fragrance, Methylparaben, Nonoxynol 9, Propylene Glycol, Propylparaben, Sodium Phosphate Dibasic, Water

Questions? 888-309-9030

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FIRST AID ANTISEPTIC 
benzalkonium 0.13%, lidocaine hcl 2.5% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41250-805
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE	25 mg  in 1 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Diazolidinyl Urea (UNII: H5RIZ3MPW4)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
Methylparaben (UNII: A2I8C7HI9T)
NONOXYNOL-9 (UNII: 48Q180SH9T)
Propylene Glycol (UNII: 6DC9Q167V3)
Propylparaben (UNII: Z8IX2SC1OH)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41250-805-04	148 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/07/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/07/2013

Labeler - Meijer (006959555)

Registrant - Product Quest Mfg (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg		927768135	manufacture(41250-805) , label(41250-805)