ALOCANE PLUS- lidocaine hydrochloride and benzalkonium chloride gel 
Quest Products, Inc.

----------

Alocane ® First Aid Antiseptic

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Lidocaine HCl 4.0%

Purpose

First Aid Antiseptic

Topical Analgesic

Uses

First Aid to help prevent bacterial infection associated with contamination of the skin. Temporarily relieves pain and itching due to:

Warnings

For external use only. Avoid contact with eyes.

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Stop use and ask doctor: if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Stop Use and ask doctor

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

Do not use:

in large quantities, particularly over raw surfaces or blistered areas.

If pregnant or breast-feeding

ask a health care professional before use.

Directions:

Adults and children 2 years of age or older:

Children under 2 years of age: consult a doctor

Other Information

Store at room temperature of 15° - 30°C (59° - 86°F)

Inactive Ingredients

1,3-Propanediol, Aloe Barbadensis (Aloe) Leaf Juice, Caprylyl Glycol, Chlorphenesin, Dimethyl Isosorbide, Hydroxyethyl Cellulose, Phenoxyethanol, Tocopheryl Acetate (Vitamin E), Water.

PRINCIPAL DISPLAY PANEL - 3.5 fl oz Spray

PDP

ALOCANE PLUS 
lidocaine hydrochloride and benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68229-404
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
PROPANEDIOL (UNII: 5965N8W85T)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
HYDROXYETHYL CELLULOSE (5500 MPA.S AT 2%) (UNII: M825OX60H9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68229-404-01104 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/03/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/03/2021
Labeler - Quest Products, Inc. (075402441)
Establishment
NameAddressID/FEIBusiness Operations
Fill Tech USA926433855manufacture(68229-404)

Revised: 11/2023
Document Id: 0a36ea8d-bd18-8b31-e063-6394a90a852f
Set id: cfe8114b-df65-064b-e053-2a95a90a33f6
Version: 3
Effective Time: 20231115
 
Quest Products, Inc.