CREAMOL ALCOHOL WIPES- alcohol swab

Creamol Alcohol Wipes by

Drug Labeling and Warnings

Creamol Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol (45%), Isopropyl Alcohol (30%), Benzalkonium Chloride (0,13%) (w/w)

PURPOSE

Antiseptic

Directions

Used for hand and skin cleaning. Open the label and take one. Gently wipe your hands with an antibacterial wipe. It does not require rinsing after use.

INDICATIONS & USAGE

It provides a practical cleaning without using water and soap when necessary. It helps reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

For external use only. Flammable, keep away from fire and flame.

DO NOT USE

Do not use on open wounds and in children less than 2 months of age

WHEN USING

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water.

STOP USE

If irritation and redness develops and persist and in case of poisoning stop use and ask a doctor. Symptoms of Poisoning are dizziness, loss of consciousness and speech disorder.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT

Aqua, Glycerine, Parfum, D-Panthenol, Tocopheryl Acetate

Other informations

Store between 15-30 ºC. Avoid freezing and excessive heat above 40ºC

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CREAMOL ALCOHOL WIPES 
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77892-0005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	45 mg  in 100 mg
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	30 mg  in 100 mg
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77892-0005-1	80 mg in 1 POUCH; Type 0: Not a Combination Product	08/24/2020
2	NDC: 77892-0005-2	150 mg in 1 POUCH; Type 0: Not a Combination Product	08/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/24/2020

Labeler - LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN (502952094)

Establishment
Name	Address	ID/FEI	Business Operations
LABER KIMYA AR-GE SANAYI TICARET - LEVENT KAHRIMAN		502952094	manufacture(77892-0005)