HAND SANITIZER- alcohol gel

国家: 美国

语言: 英文

来源: NLM (National Library of Medicine)

有效成分:

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

可用日期:

Puranic, Inc

给药途径:

EXTRACORPOREAL

处方类型:

OTC DRUG

疗效迹象:

Antiseptic, Hand Sanitizer Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. - in children less than 2 months of age - on open skin wounds Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

授权状态:

OTC monograph not final

产品特点

HAND SANITIZER- ALCOHOL GEL
PURANIC, INC
_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._
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11754-120 120 ML SHUNAN 75556-120 PURANIC, INC
ACTIVE INGREDIENT(S)
Alcohol 75% v/v. Purpose: Antiseptic
PURPOS E
Antiseptic, Hand Sanitizer
US E
Hand Sanitizer to help 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 heat or flame
DO NOT USE
in children less than 2 months of age
on open skin wounds
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
Place enough product on hands to cover all surfaces. Rub hands
together until dry.
Supervise children under 6 years of age when using this product to
avoid swallowing.
OTHER INFORMATION
Store between 59-86 (15-30 )
Avoid freezing and excessive heat above 110 (40 )
INACTIVE INGREDIENTS
Water,Glycerin,Propylene Glycol, Triethanolamine,Tocopheryl
Acetate,Aloe Barbadensis Leaf Juice
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
120 mL in 1 Bottle NDC: 11754-120-01
HAND SANITIZER
alcohol gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:11754-120
ROUTE OF ADMINISTRATION
EXTRACORPOREAL
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
9 0 mL in 120 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
TRO LAMINE (UNII: 9 O3K9 3S3TK)
.ALPHA.-TO CO PHERO L ACETATE (UNII: 9 E8 X8 0 D2L0 )
GLYCERIN (UNII: PDC6 A3C0 OX)
PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)
WATER (UNII: 0 59 QF0 KO0 R)
ALO E VERA LEAF (UNII: ZY