Label: ANTIBACTERIAL WET WIPES- benzalkonium chloride swab
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Contains inactivated NDC Code(s)
NDC Code(s): 42255-900-01 - Packager: ZHEJIANG GREENFACE HOUSEWARES CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated January 8, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Uses
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Warnings
For external use only.
When using this product do not get into eyes.
If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash
develops and continues for more than 72 hours.
Keep out of reach of children. If swallowed, get
medical help or contact a Poison Control Center
right away.
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Directions
For use apply thoroughly to hands and face as
desired. Allow to dry without wiping.
For dispensing lift tab at front of lid to open.
Pull up corner of center sheet and thread through
dispenser slit in lid. Pull out exposed wipe at a 45
angle and snap off. The next wipe is ready for
dispensing. Close lid to retain moisture. Dispose
of used wipes in trash receptacle. Do not flush.
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL WET WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42255-900 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.115 g in 100 g Inactive Ingredients Ingredient Name Strength DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CITRIC ACID ACETATE (UNII: DSO12WL7AU) EDETATE DISODIUM (UNII: 7FLD91C86K) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42255-900-01 75 in 1 PACKAGE 01/08/2018 1 1.875 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/14/2013 Labeler - ZHEJIANG GREENFACE HOUSEWARES CO., LTD. (546596567) Establishment Name Address ID/FEI Business Operations ZHEJIANG GREENFACE HOUSEWARES CO., LTD. 527999264 manufacture(42255-900)