SERVO-STAT P- chloroxylenol liquid

Servo-Stat P by

Drug Labeling and Warnings

Servo-Stat P by is a Otc medication manufactured, distributed, or labeled by Enzyme Solutions, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

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

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use

for hand-washing to decrease bacteria on the skin

WARNINGS

Warnings

For external use only

When using this product

Do not get in eyes

If 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

DOSAGE & ADMINISTRATION

Directions

Ready to use

Do not dilute

Wet hands and forearms

Apply 5 milliliters (palmful) to hands and forearms

Rinse thoroughly

INACTIVE INGREDIENT

Ingredients

Water, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Cocamidopropylbetaine, Tetrasodium EDTA, Propylene Glycol, Fragrance, Sodium Chloride, Boric Acid, Glycol Stearate, PEG-75 Lanolin, DMDM Hydantoin, Aloe Vera, FDC Red #40, FDC Yellow #6

PRINCIPAL DISPLAY PANEL

Servo-Stat P

Antiseptic Hand Wash

11106R-A1000

1000 ml (33.8 fl oz.)

INGREDIENTS AND APPEARANCE

SERVO-STAT P 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76378-017
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)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
EDETATE SODIUM (UNII: MP1J8420LU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BORIC ACID (UNII: R57ZHV85D4)
GLYCOL STEARATE (UNII: 0324G66D0E)
PEG-75 LANOLIN (UNII: 09179OX7TB)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76378-017-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/07/2018
2	NDC: 76378-017-02	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/07/2018
3	NDC: 76378-017-03	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/07/2018
4	NDC: 76378-017-04	1000 mL in 1 BAG; Type 0: Not a Combination Product	12/07/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/01/2011

Labeler - Enzyme Solutions, Inc. (004994559)

Establishment
Name	Address	ID/FEI	Business Operations
Enzyme Solutions, Inc.		004994559	manufacture(76378-017)