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

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Alocane ® Max Spray

Drug Facts

Active IngredientPurpose

Benzalkonium Chloride 0.13%

Lidocaine HCL 4%

First Aid Antiseptic

Topical Analgesic

Uses:

First aid to help prevent bacterial icontamination or skin infection, and for 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. Spray a small amount on the affected area 3 to 4 times daily. May be covered with a sterile bandage (let dry first). To apply to the face, spray on palm and apply.

Children under 2 years of age: ask a doctor.

Other Information

Store at 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 - 3.5 fl oz spray

3.5ozPDP

ALOCANE MAX 
lidocaine hydrochloride and benzalkonium chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68229-408
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:68229-408-01104 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/15/2023
2NDC:68229-408-02118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/15/2023
3NDC:68229-408-03124 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/15/2023
Labeler - Quest Products LLC (075402441)
Establishment
NameAddressID/FEIBusiness Operations
Filltech USA, LLC926433855manufacture(68229-408)

Revised: 11/2023
Document Id: 0a35221a-2fcc-2735-e063-6294a90a88ca
Set id: 0a35221a-2fcb-2735-e063-6294a90a88ca
Version: 1
Effective Time: 20231115
 
Quest Products LLC