XTRA- benzalkonium chloride spray

XTRA by

Drug Labeling and Warnings

XTRA by is a Otc medication manufactured, distributed, or labeled by Zhejiang Jifu Daily Chemical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

for handwashing, to reduce bacteria on skin

Warnings

For external use only.

Keep out of reach of children

Keep out of reach of children

Do not use

Do not use with chlorine bleach to avoid irritating fumes.

Avoid contact with eyes.

If eye contact occures fush thoroughly with water.

Do not ingest

Do not ingest. If ingested, drink plenty of water, contact a physician.

STORAGE AND HANDLING

Store in a cool and dry pleace, and avoid direct sunlight.

Directions

Spray to wet hand. Scrub and rinse thoroughly.

Inactive ingredients

Water (Aqua）

Sodium Laureth Sulfate

Decyl Glucoside

Citric Acid

Methylisothiazlione

Phenoxyethanol

Sodium Benzoate

Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XTRA 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84987-001
Route of Administration	SUPRACHOROIDAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRIC ACID (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Product Characteristics
Color		Score
Shape		Size
Flavor	ORANGE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84987-001-01	399 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	11/27/2024

Labeler - Zhejiang Jifu Daily Chemical Co., Ltd. (710111693)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Jifu Daily Chemical Co., Ltd.		710111693	manufacture(84987-001) , label(84987-001)