Label: SECURO HAND SANITIZER- benzethonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 75990-370-01, 75990-370-03, 75990-370-05, 75990-370-06, view more75990-370-07, 75990-370-08, 75990-370-09, 75990-370-10, 75990-370-11, 75990-370-12, 75990-370-13, 75990-370-14, 75990-370-15, 75990-370-16, 75990-370-17, 75990-370-18, 75990-370-19, 75990-370-20, 75990-370-24, 75990-370-27, 75990-370-28, 75990-370-35, 75990-370-55 - Packager: Certus Medical, Inc.
- 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 March 14, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
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- Drug Facts Box OTC-Active Ingredient Section
- Drug Facts Box OTC-Purpose Section
- Drug Facts Box OTC-Indications & Usage Section
- Drug Facts Box OTC-Warnings Section
- Drug Facts Box OTC-When Using Section
- Drug Facts Box OTC-Stop Use Section
- Drug Facts Box OTC-Keep Out of Reach of Children Section
- Drug Facts Box OTC-Dosage & Administration Section
- Drug Facts Box OTC-Inactive Ingredient Section
- 6370 Securo Hand Sanitizer
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INGREDIENTS AND APPEARANCE
SECURO HAND SANITIZER
benzethonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75990-370 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) DMDM HYDANTOIN (UNII: BYR0546TOW) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75990-370-06 1 in 1 BOX 03/14/2017 1 800 mL in 1 BAG; Type 0: Not a Combination Product 2 NDC:75990-370-17 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 3 NDC:75990-370-24 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 4 NDC:75990-370-01 1200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 03/14/2017 5 NDC:75990-370-03 350 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 03/14/2017 6 NDC:75990-370-05 540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 7 NDC:75990-370-07 700 mL in 1 BAG; Type 0: Not a Combination Product 03/14/2017 8 NDC:75990-370-09 2000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 03/14/2017 9 NDC:75990-370-10 1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 03/14/2017 10 NDC:75990-370-11 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 11 NDC:75990-370-12 1000 mL in 1 BAG; Type 0: Not a Combination Product 03/14/2017 12 NDC:75990-370-13 800 mL in 1 BAG; Type 0: Not a Combination Product 03/14/2017 13 NDC:75990-370-14 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 14 NDC:75990-370-15 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 15 NDC:75990-370-28 149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 16 NDC:75990-370-27 800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 03/14/2017 17 NDC:75990-370-55 208200 mL in 1 DRUM; Type 0: Not a Combination Product 03/14/2017 18 NDC:75990-370-08 1 in 1 BOX 03/14/2017 18 1000 mL in 1 BAG; Type 0: Not a Combination Product 19 NDC:75990-370-16 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 20 NDC:75990-370-18 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/14/2017 21 NDC:75990-370-19 18900 mL in 1 CONTAINER; Type 0: Not a Combination Product 03/14/2017 22 NDC:75990-370-20 75600 mL in 1 DRUM; Type 0: Not a Combination Product 03/14/2017 23 NDC:75990-370-35 132500 mL in 1 DRUM; Type 0: Not a Combination Product 03/14/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/14/2017 Labeler - Certus Medical, Inc. (966433653) Establishment Name Address ID/FEI Business Operations ABC Compounding Co., Inc. 003284353 manufacture(75990-370)