DEFENDMAX SANITIZING WIPES- alcohol cloth

Maa: Yhdysvallat

Kieli: englanti

Lähde: NLM (National Library of Medicine)

Aktiivinen ainesosa:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Saatavilla:

Etailer Limited

Antoreitti:

TOPICAL

Prescription tyyppi:

OTC DRUG

Käyttöaiheet:

Antiseptic Decreases bacteria on skin. - in children less than 2 months of age - on open skin wounds - if you are allergic to any of the ingredients Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Valtuutuksen tilan:

OTC monograph not final

Valmisteyhteenveto

DEFENDMAX SANITIZING WIPES- ALCOHOL CLOTH
ETAILER LIMITED
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
----------
DEFENDMAX SANITIZING WIPES (CLOTH) NDC: 78256-105-10
ACTIVE INGREDIENT(S)
Ethanol 75% v/v
PURPOS E
Antiseptic
US E(S )
Decreases bacteria on skin.
WARNINGS
For external use only. Flammable. Keep away from heat or flame
DO NOT USE
in children less than 2 months of age
on open skin wounds
if you are allergic to any of the ingredients
When using this product keep out of eyes, ears, and mouth. In case of
contact with eyes, rinse eyes
thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be
signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control Center right
away.
DIRECTIONS
Apply to Hands
Wet hands thoroughly with product and allow to dry without wiping.
OTHER INFORMATION
Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)
INACTIVE INGREDIENTS
Glycerin, Vitamin E, Water
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
DISTRIBUTED BY:
DEFENDMAX
99 WALL STREET # 570
NEW YORK, NY 10005
UNITED STATES OF AMERICA
_DEFENDMAX SANATIZING WIPES (CLOTH - 100 CT) NDC: 78256-105-10_
DEFENDMAX SANITIZING WIPES
alcohol cloth
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:78 256 -10 5
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
75 g in 10 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
.ALPHA.-TO CO PHERO L (UNII: H4N8 55PNZ1)
GLYCERIN (UNII: PDC6 A3C0 OX)
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:78 256 -10 5-10
48 0 g in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct
0 9 /30 /20 20
Etailer Limited