OLJE ANTIBACTERIAL WIPES- benzalkonium chloride swab

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

AJ Co., Ltd.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

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.

Authorization status:

OTC monograph not final

Summary of Product characteristics

OLJE ANTIBACTERIAL WIPES- BENZALKONIUM CHLORIDE SWAB
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._
----------
AJ CO., LTD. - OLJE ANTIBACTERIAL WIPES
Benzalkonium Chloride
water, 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
OLJE ANTIBACTERIAL WIPES
benzalkonium chloride swab
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:75356 -0 0 0 3
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 .0 0 0 4 g
in 0 .4 g
AJ Co., Ltd.
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
.ALPHA.-TO CO PHERO L ACETATE (UNII: 9 E8 X8 0 D2L0 )
EDETATE DISO DIUM ANHYDRO US (UNII: 8 NLQ36 F6 MM)
CITRIC ACID MO NO HYDRATE (UNII: 29 6 8 PHW8 QP)
TEA TREE O IL (UNII: VIF56 5UC2G)
PO LYSO RBATE 2 0 (UNII: 7T1F30 V5YH)
PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)
PHENO XYETHANO L (UNII: HIE49 2ZZ3T)
SO DIUM CITRATE (UNII: