ANTISEPTIC HAND WIPES - benzalkonium chloride swab 
Natrual Products 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.

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Antiseptic Hand Wipes

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1 percent

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin

Warnings

For external use only

Do not use

in the eyes. In case of contact, flush thoroughly iwth water.

Stop use and ask a doctor if irritation and redness develop.

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

Wet hand thoroughly with product and allow to dry without wiping.

Other Information Dispose in normal household waste. Do not flush down the toilet. Reseal pack to maintain moisture.

Inactive ingredients Water, glycerin, aloe vera leaf juice, propylene glycol, phenoxyethanol, diazolidinyl urea, lauryl glucoside, disodium EDTA, sodium citrate, maltodextrin, fragrance

Distributed By: NATURAL PRODUCTS LTD, 3 WARPLE WAY, LONDON W3 ORX, NPW.CO.UK

IN USA: 1205 HILLTOP PARKWAY

STEAMBOAT SPRINGS, CO, 80487, NPW-USA.COM

MADE IN CHINA



npw

moisturizing
kills germs

5 wipes

ANTISEPTIC HAND WIPES

cleans and refreshes hands without soap and water

NET WT. 0.35 OZ (10 G)


53102-000-00 label

53102-000-01 label

ANTISEPTIC HAND WIPES  
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:53102-000
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
ALOE VERA LEAF 
PROPYLENE GLYCOL 
PHENOXYETHANOL 
DIAZOLIDINYL UREA 
LAURYL GLUCOSIDE 
EDETATE DISODIUM 
SODIUM CITRATE 
MALTODEXTRIN 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53102-000-005 in 1 BAG
11.9 mL in 1 PACKET
2NDC:53102-000-015 in 1 BAG
21.9 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E09/27/201203/10/2014
Labeler - Natrual Products Ltd (233517341)
Registrant - Yangzhou Perfect Daily Chemicals Co., Ltd (529256861)
Establishment
NameAddressID/FEIBusiness Operations
Yangzhou Perfect Daily Chemicals Co., Ltd529256861manufacture(53102-000)

Revised: 3/2014
 
Natrual Products Ltd