Active ingredients

Benzalkonium Cl 0.13%

Lidocaine HCl 4%

Purpose

Benzalkonium Cl – First Aid Antiseptic

Lidocaine HCl – 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 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; spray a small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first)
children under 2 years: ask a doctor

Other Safety Information

store at room temperature
avoid excessive heat

Inactive ingredients

chlorphenesin, edetate disodium, fragrance, glycerin, nonoxynol 9, phenoxyethanol, propylene glycol, purified water

Questions

888-309-9030

Package/Label Principal Display Panel

Principal Display Panel

DG HEALTH MAXIMUM STRENGTH PAIN RELIEVING CLEANSING
benzalkonium cl, lidocaine hcl spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75712-200
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	40 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CHLORPHENESIN (UNII: I670DAL4SZ)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
NONOXYNOL-9 (UNII: 48Q180SH9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:75712-200-01	148 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/11/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	02/11/2022

Labeler - Dollar General Corporation (006946172)

Drug Facts