ALOCANE PLUS- lidocaine hydrochloride and benzalkonium chloride gel

Alocane Plus by

Drug Labeling and Warnings

Alocane Plus by is a Otc medication manufactured, distributed, or labeled by Quest Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredient	Purpose
Benzalkonium Chloride 0.13% Lidocaine HCL 4%	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:

• Minor Burns
• Minor Cuts & Scrapes
• Minor Skin Irritations

Warnings

For external use only. Avoid contact with eyes.

Keep out of reach of children. In case of accidental ingestion, seek medical help or call 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.

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

Directions

Adults and children 2 years of age and older: Apply to affected areas not more than 3 to 4 times daily.

Children under 2 years of age: consult a doctor.

Other Information

Store at room temperature 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 - 48 packet carton

INGREDIENTS AND APPEARANCE

ALOCANE PLUS 
lidocaine hydrochloride and benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68229-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 g  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68229-300-06	48 in 1 CARTON	11/12/2020
1	NDC: 68229-300-05	3.55 mL in 1 DOSE PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/01/2020

Labeler - Quest Products LLC (075402441)