XTRA ANTIBACTERIAL HAND JUICY ORANGE- chloroxylenol gel

Xtra Antibacterial Hand Juicy Orange by

Drug Labeling and Warnings

Xtra Antibacterial Hand Juicy Orange by is a Otc medication manufactured, distributed, or labeled by MY IMPORTS USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Uses

• for handwashing, to reduce bacteria on skin

Warnings

For external use only.

Keep out of reach of children.

Avoid contact with eyes. If eye contact occures flush thoroughly with water. Do not ingest. If ingested, drink plenty of water, contact a physician.

Directions

• Apply palmful to wet hands. Scrub and rinse thoroughly.

Inactive Ingredients

Deionized Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Glycerin, Fragrance, Sodium Hydroxide, Lactic Acid, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, FD&C yellow no.5, FD&C red no.40

Questions/Comments?

Call toll-free 1-877-879-6999 or email us at info@amgbrandsllc.com

Package Labeling:

INGREDIENTS AND APPEARANCE

XTRA ANTIBACTERIAL HAND JUICY ORANGE 
chloroxylenol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51628-0033
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51628-0033-0	709 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/01/2023

Labeler - MY IMPORTS USA, LLC (195767988)