ALOCANE MAX- lidocaine hydrochloride and benzalkonium chloride gel 
Quest Products LLC

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Alocane ® Max gel

Drug Facts

Active IngredientPurpose

Benzalkonium Chloride 0.13%

Lidocaine HCL 4%

First Aid Antiseptic

Topical Analgesic

Uses:

First aid to help prevent bacterial infection associated with contamination or skin infection, and for the temporary relief of pain and itching associated with minor: :

Warnings

For external use only.

Ask a doctor before use if you have:

  • Deep or puncture wounds
  • Animal bites
  • Serious burns

Do not use:

  • In or near the eyes
  • In large quantities or over large areas of the body
  • On raw surfaces or blistered areas

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.

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

Directions:

Adults and children 2 years of age and older: Clean the affected area. Apply a small amounbt of gel on the affected area not more than 3 to 4 times daily. May be covered with a sterile bandgae (let dry first).

Children under 2 years of age: ask a doctor.

Other Information

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

Inactive Ingredients

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

PRINCIPAL DISPLAY PANEL - 2.5 fl oz tube

2.5ozTube

24 count single use

24sachet

ALOCANE MAX 
lidocaine hydrochloride and benzalkonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68229-406
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
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)  
PROPANEDIOL (UNII: 5965N8W85T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68229-406-021 in 1 CARTON11/15/2023
1NDC:68229-406-0175 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:68229-406-051 in 1 CARTON11/15/2023
2NDC:68229-406-03118 mL in 1 TUBE; Type 0: Not a Combination Product
3NDC:68229-406-0724 in 1 CARTON11/15/2023
3NDC:68229-406-063.4 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01705/01/2020
Labeler - Quest Products LLC (075402441)

Revised: 1/2024
Document Id: 0fdb29cc-a912-0801-e063-6294a90acdd8
Set id: 0a33f9a9-1fdc-7cdf-e063-6294a90adca1
Version: 2
Effective Time: 20240126
 
Quest Products LLC