PROGRESS ANTIBACTERIAL WIPES LEMON SCENT- benzalkonium chloride cloth

Progress Antibacterial Wipes Lemon Scent by

Drug Labeling and Warnings

Progress Antibacterial Wipes Lemon Scent by is a Otc medication manufactured, distributed, or labeled by Truechoicepack, Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Uses

• For hand sanitizing to decrease bacteria on the skin.
• Apply topically to the skin to help prevent cross contamination.
• Recommended for repeated use.
• Dries in seconds.

Warnings

For external use only.

When using this product

do not use in or contact the eyes.

Stop use and ask a doctor is

too much skin irritation or sensitivity develops or increases.

Keep this out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• Gently pull back resealable label, remove and use wipe as required.
• Reseal back after use.

Other information

• Lot No. Manufacture date and Expiration date can be found on package.

Inactive Ingredients

Water, Phenoxyethanol, DMDM Hydantoin, Polysorbate 20, Ethylparaben, Methylparaben, Disodium Citrate, Aloe Barbadensis Leaf Juice, Parfum

Package Labeling:

INGREDIENTS AND APPEARANCE

PROGRESS ANTIBACTERIAL WIPES LEMON SCENT 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80882-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DMDM HYDANTOIN (UNII: BYR0546TOW)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ETHYLPARABEN (UNII: 14255EXE39)
METHYLPARABEN (UNII: A2I8C7HI9T)
DISODIUM HYDROGEN CITRATE (UNII: 6FO62KCQ7A)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80882-002-50	50 in 1 BAG	11/20/2020
1		4.04 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/20/2020

Labeler - Truechoicepack, Corp (078786060)