Label: COVEX ANTIBACTERIAL BAR ACTIVE PROTECTION- benzalkonium chloride soap
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Contains inactivated NDC Code(s)
NDC Code(s): 51209-021-27, 51209-021-90 - Packager: DALAN KIMYA ENDUSTRI ANONIM SIRKETI
- 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 February 24, 2021
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
- Directions
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Inactive ingredients:
Sodium Tallowate, Sodium Palmate, Water, Sodium Palm Kernelate, Fragrance, Sodium Chloride, Glycerine, Zinc Oxide, C12-15 Alkyl Lactate, Titanium Dioxide, Tetrasodium EDTA, Etidronic Acid, Disodium Distyrylbiphenyl Disulfonate, Limonene, Linalool, Hexyl Cinnamal, Benzyl Salicylate, Geraniol, Eugenol.
- Package Labeling:51209-021-90
- Package Labeling:51209-021-27
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INGREDIENTS AND APPEARANCE
COVEX ANTIBACTERIAL BAR ACTIVE PROTECTION
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51209-021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 g Inactive Ingredients Ingredient Name Strength SODIUM TALLOWATE, BEEF (UNII: 07RIK6QMEW) SODIUM PALMATE (UNII: S0A6004K3Z) WATER (UNII: 059QF0KO0R) SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) SODIUM CHLORIDE (UNII: 451W47IQ8X) GLYCERIN (UNII: PDC6A3C0OX) ZINC OXIDE (UNII: SOI2LOH54Z) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) EDETATE SODIUM (UNII: MP1J8420LU) ETIDRONIC ACID (UNII: M2F465ROXU) DISODIUM DISTYRYLBIPHENYL DISULFONATE (UNII: 81G7704MYR) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+/-)- (UNII: D81QY6I88E) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) BENZYL SALICYLATE (UNII: WAO5MNK9TU) GERANIOL (UNII: L837108USY) EUGENOL (UNII: 3T8H1794QW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51209-021-90 90 g in 1 BOX; Type 0: Not a Combination Product 02/24/2021 2 NDC:51209-021-27 270 g in 1 PACKAGE; Type 0: Not a Combination Product 02/24/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/24/2021 Labeler - DALAN KIMYA ENDUSTRI ANONIM SIRKETI (566219285)