SANIPRO DISINFECTANT WIPES- benzalkonium chloride liquid

Land: USA

Språk: engelska

Källa: NLM (National Library of Medicine)

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Ladda ner Produktens egenskaper (SPC)
19-08-2020

Aktiva substanser:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Tillgänglig från:

AJ Co., Ltd.

Administreringssätt:

TOPICAL

Receptbelagda typ:

OTC DRUG

Terapeutiska indikationer:

Antibacterial Wipes to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Thoroughly wipe hands with wipe. Discard properly. Not flushable. Be sure to close lid to keep wipes moist.

Bemyndigande status:

OTC monograph not final

Produktens egenskaper

                                SANIPRO DISINFECTANT WIPES- BENZALKONIUM CHLORIDE LIQUID
AJ CO., LTD.
_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._
----------
Benzalkonium Chloride
Propylene Glycol
Phenoxyethanol
Glycerin
Sodium Benzoate
Sodium Citrate
Disodium EDTA
Polysorbate 20
Citric Acid
Melaleuca Alternifolia (Tea Tree) Leaf Oil
Tocopheryl Acetate
Antibacterial Wipes to help reduce bacteria that potentially can cause
disease. For use when soap and
water are not available.
keep out of reach of the children
Thoroughly wipe hands with wipe.
Discard properly. Not flushable.
Be sure to close lid to keep wipes moist.
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
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.
for external use only
SANIPRO DISINFECTANT WIPES
benzalkonium chloride liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:75356 -0 0 0 4
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6 JUD5X6 Y)
BENZALKONIUM
CHLORIDE
0 .1 g
in 10 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:75356 -0 0 0 4-1
40 0 g in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct
0 8 /0 8 /20 20
2
NDC:75356 -0 0 0 4-2
8 0 g in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct
0 8 /0 8 /20 20
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
                                
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