Label: ANTIBACTERIAL WET WIPES- benzalkonium chloride swab
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Contains inactivated NDC Code(s)
NDC Code(s): 59575-501-01, 59575-501-02, 59575-501-03, 59575-501-04 - Packager: Hebei Yihoucheng Commodity 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 August 24, 2013
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Use
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Warnings
For external use only.
Do not use over large areas of the body
if you are allergic to any of the ingredients.
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. - Directions
- 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:59575-501 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 PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALCOHOL (UNII: 3K9958V90M) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) TOCOPHEROL (UNII: R0ZB2556P8) QUATERNIUM-22 (UNII: MXO138JCBP) PEG-60 CASTOR OIL (UNII: VXP26NM2XX) CITRACONIC ACID (UNII: 0RQ6CXO9KD) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59575-501-03 3 in 1 BAG 1 10 in 1 PACKAGE 1 3 g in 1 POUCH 2 NDC:59575-501-04 20 in 1 BOX 2 1 in 1 PACKAGE 2 3 g in 1 POUCH 3 NDC:59575-501-01 10 in 1 PACKAGE 3 3 g in 1 POUCH 4 NDC:59575-501-02 1 in 1 PACKAGE 4 3 g in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/16/2013 Labeler - Hebei Yihoucheng Commodity Co.,Ltd. (529305333) Establishment Name Address ID/FEI Business Operations Hebei Yihoucheng Commodity Co.,Ltd. 529305333 manufacture(59575-501)
