PAIN RELIEVING ANTISEPTIC- benzalkonium chloride, lidocaine hydrochloride spray

Pain Relieving Antiseptic by

Drug Labeling and Warnings

Pain Relieving Antiseptic by is a Otc medication manufactured, distributed, or labeled by Walmart, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

• Active ingredients: Purpose
• Benzalkonium CI 0.13% w/w: First aid antiseptic
• Lidocaine HCI 4% w/w: Pain reliever

INACTIVE INGREDIENT

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

Uses

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

■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 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.

DOSAGE & ADMINISTRATION

Drections 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 SAFETY INFORMATION

Other information Protect from excessive heat.

INACTIVE INGREDIENT

Inactive ingredients Camphor, Deionized water, Propylene glycol

QUESTIONS

Questions? 1-888-287-1915

PURPOSE

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

PRINCIPAL DISPLAY PANEL

NDC# 79903-234-01

5 FL OZ (148 mL)

INGREDIENTS AND APPEARANCE

PAIN RELIEVING ANTISEPTIC 
benzalkonium chloride, lidocaine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-234
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 g  in 100 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CAMPHOR, (-)- (UNII: 213N3S8275)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-234-01	148 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	02/29/2024

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

Labeler - Walmart, Inc. (051957769)