MICRO-ASEPTIC- chloroxylenol liquid

Micro-Aseptic by

Drug Labeling and Warnings

Micro-Aseptic by is a Otc medication manufactured, distributed, or labeled by ASEPTIC CONTROL PRODUCTS, INC., Enzyme Solutions, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

PCMX (para-chloro-meta-xylenol) 0.6%

Purpose

Antimicrobial

Use

for hand-washing to decrease bacteria on the skin

Warnings

For external use only

When using this product

• do not get into eyes
• of contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation and redness develop

Keep out of reach of children.

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

Directions

• ready to use
• do not dilute
• wet hands and forearms
• apply 5 milliters (teaspoonful) or palmful to hands and forearms
• scrub thoroughly for 1 minute and rinse

Inactive Ingredients

Water, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Cocamidopropylbetaine, Propylene Glycol, Tetrasodium EDTA, Isopropanol, Lauramine oxide, Boric Acid, PEG-75 Lanolin, DMDM Hydantoin, Fragrance, Aloe Vera, FD&C Blue #1, FD&C Yellow #5

PRINCIPAL DISPLAY PANEL

Micro-

Aseptic

Antimicrobial

Skin Cleanser

NDC # 81591-001-02

Manufactured for

ASEPTIC CONTROL PRODUCTS, INC

1225 Carnegie Street, Unit 104

Rolling Meadows, IL 60008

Made in the U.S.A.

Item #: 1955-16OZ

473 ml (16 FL. OZ.)

INGREDIENTS AND APPEARANCE

MICRO-ASEPTIC 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81591-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PEG-75 LANOLIN (UNII: 09179OX7TB)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
EDETATE SODIUM (UNII: MP1J8420LU)
BORIC ACID (UNII: R57ZHV85D4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81591-001-01	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/26/2021
2	NDC: 81591-001-02	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/26/2021
3	NDC: 81591-001-03	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/26/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/26/2021

Labeler - ASEPTIC CONTROL PRODUCTS, INC. (161977020)

Establishment
Name	Address	ID/FEI	Business Operations
Enzyme Solutions, Inc.		004994559	manufacture(81591-001)