Label: STERIZAR ADVANCED BARRIER CONTROL- benzalkonium chloride spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79310-304-21, 79310-304-22, 79310-304-23, 79310-304-25 - Packager: Unicorn Media Partners LLC
- 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 November 4, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
- Purpose
- Use(s)
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Warnings
For external use only. Keep away from heat. Flammable, Keep Away from Heat and Flame
When using this product keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label
NDC 79310-304-23
STERiZAR®
Advanced Barrier ControlHand Foam
SanitizerSpecially formulated to kill
harmful bacteria in secondsALCOHOL
FREEKills 99.999% of germs
Remains effective after application for at
least 6 hours using Advanced Barrier Control.
No need to rinse. Moisturizing foam that
is kind to your hands.3.4 FL OZ (100 mL)
• HALAL MONITORING •
COMMITTEE - UK -
INGREDIENTS AND APPEARANCE
STERIZAR ADVANCED BARRIER CONTROL
benzalkonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79310-304 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride 16 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) SODIUM ETHASULFATE (UNII: 12838560LI) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79310-304-25 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 2 NDC:79310-304-23 100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 3 NDC:79310-304-22 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 4 NDC:79310-304-21 5000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333A 11/01/2020 Labeler - Unicorn Media Partners LLC (117525623)