WHENEVER HAND PURIFYING- ethanol gel

Krajina: Spojené štáty

Jazyk: angličtina

Zdroj: NLM (National Library of Medicine)

Aktívna zložka:

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

Dostupné z:

JoyunCostech

Spôsob podávania:

TOPICAL

Typ predpisu:

OTC DRUG

Terapeutické indikácie:

Antiseptic ■ Hand sanitizer to decrease bacteria on hands which may cause disease

Stav Autorizácia:

OTC monograph not final

Súhrn charakteristických

WHENEVER HAND PURIFYING- ETHANOL GEL
JOYUNCOS TECH
_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._
----------
ACTIVE INGREDIENT
Ethanol 62 % v/v
INACTIVE INGREDIENTS
D.I Water, Glycerin, 1.3BG, Cabopol EEG 940, Sodium Hyaluronate(0.5%),
Aloe Extract,
Tromethamine(20%)
PURPOSE
Antiseptic
WARNINGS
For external use only-hands
Flammable. Please keep away from heat and flame.
When using this product ■ Keep out of eyes. In case of contact with
eyes, flush thoroughly with water.
■ Avoid contact with damaged skin. ■ Do not inhale or ingest.
Stop use and ask a doctor if skin irritation or rash develops.
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control Center
immediately.
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
immediately.
US ES
■ Hand sanitizer to decrease bacteria on hands which may cause
disease
DIRECTIONS
■ Squeeze out the contents from the pack and rub softly on hands to
cover all surfaces and nails.
Continue rub hands smoothly until they dried.
■ Supervise thoroughly children when they use not to swallowing.
OTHER INFORMATION
■ Store between 50F~86F (10C~30C)
■ Avoid freezing and excessive heat above 40C (104F)
QUESTIONS
If you have any question about this product, please phone to
[phone] or email to;
[e-mail]
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
WHENEVER HAND PURIFYING
ethanol gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:9 0 0 38 -0 10
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
6 2 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WA TER (UNII: 0 59 QF0 KO0 R)
GLYCERIN (UNII: PDC6 A3C0 OX)
HYALURO NATE SO DIUM (UNII: YSE9 PPT4TH)
ALO E (