ASEPSO FRESH SCENTED ANTISEPTIC- chloroxylenol soap

Asepso Fresh Scented Antiseptic by

Drug Labeling and Warnings

Asepso Fresh Scented Antiseptic by is a Otc medication manufactured, distributed, or labeled by CODAA SWITZERLAND AG. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Chloroxylenol 0.25%

Purpose

Antiseptic

Use

• For hand washing to decrease bacteria on the skin.

Warnings

For external use only

Do not use

in the eyes

Stop use and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

• Wet hands and forearms. Apply a palmful to hands and forearms. Scrub thoroughly for 30-60 seconds. Rinse and repeat.

Other information

• Do not use on fabrics. Store away from heat and humidity

Inactive ingredients

Sodium Palmitate, Sodium Palm Kernelate, Water, Fragrance, Palm Acid, Glycerin, Sodium Chloride, Liquid Paraffin, Palm Kernel Acid, Orange Fruit Extract, Titanium Dioxide Color, Tetrasodium EDTA, Tetrasodium (1-hydroxyethylidene) Bisphosphonate, Etidronate Disodium, D&C Orange No 4.

Package Labeling:

INGREDIENTS AND APPEARANCE

ASEPSO FRESH SCENTED ANTISEPTIC 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49698-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	2.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM PALMITATE (UNII: JQ43KP6296)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
WATER (UNII: 059QF0KO0R)
PALM ACID (UNII: B6G0Y5Z616)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MINERAL OIL (UNII: T5L8T28FGP)
PALM KERNEL ACID (UNII: 79P21R4317)
ORANGE (UNII: 5EVU04N5QU)
EDETATE SODIUM (UNII: MP1J8420LU)
ETIDRONATE DISODIUM (UNII: M16PXG993G)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49698-008-01	1 in 1 CARTON	09/12/2023
1		80 g in 1 CASE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/12/2023

Labeler - CODAA SWITZERLAND AG (483467697)