CVS PAIN RELIEVING FIRST AID ANTISEPTIC- lidocaine hydrochloride, benzalkonium chloride spray

CVS Pain Relieving First Aid Antiseptic by

Drug Labeling and Warnings

CVS Pain Relieving First Aid Antiseptic by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Benzalkonium Cl 0.13% w/w

Lidocaine HCl 2.5% w/w

Purpose

First aid antiseptic

Pain reliever

Uses

Firs aid to help prevent bacterial contamination or skin infections, and temporary relief of pain and itching associated with minor:

cuts
scrapes
burns
sunburns
skin irritations

Warnings

For external use only

Ask doctor before use if you have

deep or puncture wounds
animal bites
serious burns

When using this product

do not use near the eyes
do not apply over large areas 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 a small amount on the area 1 to 3 times daily.
may be covered with a sterile bandage
if bandaged, let dry first.

Other Information

Protect from excessive heat.

Questions or comments

1-800-635-3696

Inactive Ingredients

Camphor, Deionized Water, Propylene Glycol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS PAIN RELIEVING FIRST AID ANTISEPTIC 
lidocaine hydrochloride, benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-615
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE	0.025 g  in 1 g
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-615-01	147.85 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/15/2014

Labeler - CVS Pharmacy (062312574)