TRITON HAND SANITIZER GEL- alcohol gel

Land: Verenigde Staten

Taal: Engels

Bron: NLM (National Library of Medicine)

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Download Productkenmerken (SPC)
20-12-2022

Werkstoffen:

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

Beschikbaar vanaf:

Fluid USA Inc.

Toedieningsweg:

TOPICAL

Prescription-type:

OTC DRUG

therapeutische indicaties:

Purpose: Antiseptic Hand sanitizer gel to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Autorisatie-status:

OTC monograph not final

Productkenmerken

                                TRITON HAND SANITIZER GEL- ALCOHOL GEL
FLUID USA 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._
----------
TRITON HAND SANITIZER GEL
ACTIVE INGREDIENT(S)
Active Ingredient(s): Ethanol 70 % v/v
PURPOSE
Purpose: Antiseptic
USE(S)
Hand sanitizer gel 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
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
Fold, snap, then squeeze to dispense product.
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 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)
INACTIVE INGREDIENTS
Purified Water, Propylene Glycol, Carbomer 941, Aminomethyl Propanol,
Isopropyl
Myristate, Imidazolidinyl Urea, t-Butyl Alcohol and/or Denatonium
Benzoate
PACKAGE LABEL. PRINCIPAL DISPLAY PANEL [CLEAN SHOT - PRIMARY
PACKAGING]
NDC 76944-123-01
0.05 fl. oz (1.5 mL)
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL [BAG]
250 x 0.05 fl. oz (1.5 mL) Single-Use Packets.
NDC 76944-123-03
PACKAGE LABEL. PRINCIPAL DISPLAY PANEL [PAIL]
5 gallon (20L container of 3,000 x 0.05 fl. oz (1.5 mL) Single-Use
Packets.
NDC 76944-123-04
PACKAGE LABEL. PRINCIPAL DISPLAY PANEL [BOX]
250 x 0.05 fl. oz (1.5 mL) Single-Use Packets.
NDC 76944-123-02
TRITON HAND SANITIZER GEL
alcohol gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:76944-123
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90
                                
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