Label: HAND WIPES- benzalkonium chloride swab
- NDC Code(s): 82447-101-01
- Packager: Meizhou Jubona Technology 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 December 13, 2021
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses:
- WARNINGS
- Directions
- Inactive Ingredients:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82447-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength benzalkonium chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) benzalkonium chloride 0.13 g in 100 g Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) CHLORPHENESIN CARBAMATE (UNII: 57U5YI11WP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82447-101-01 1.7 g in 1 PACKAGE; Type 0: Not a Combination Product 12/13/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/13/2021 Labeler - Meizhou Jubona Technology Co., Ltd. (712379455) Establishment Name Address ID/FEI Business Operations Meizhou Jubona Technology Co., Ltd. 712379455 MANUFACTURE(82447-101)