Label: CELOX ULTRA- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 75990-007-01, 75990-007-03, 75990-007-05, 75990-007-06, view more75990-007-07, 75990-007-08, 75990-007-09, 75990-007-10, 75990-007-11, 75990-007-12, 75990-007-13, 75990-007-14, 75990-007-15, 75990-007-16, 75990-007-17, 75990-007-18, 75990-007-24, 75990-007-27, 75990-007-28, 75990-007-30, 75990-007-55 - Packager: Certus Medical, Inc.
- Category: HUMAN OTC DRUG LABEL
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 April 25, 2011
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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
- Celox Ultra 6968 1000ml bag
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INGREDIENTS AND APPEARANCE
CELOX ULTRA
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75990-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75990-007-06 1 in 1 BOX 1 800 mL in 1 BAG 2 NDC:75990-007-30 473 mL in 1 BOTTLE, PLASTIC 3 NDC:75990-007-24 118 mL in 1 BOTTLE, PLASTIC 4 NDC:75990-007-01 1200 mL in 1 CARTRIDGE 5 NDC:75990-007-03 350 mL in 1 CARTRIDGE 6 NDC:75990-007-05 540 mL in 1 BOTTLE, PLASTIC 7 NDC:75990-007-07 700 mL in 1 BAG 8 NDC:75990-007-09 2000 mL in 1 CARTRIDGE 9 NDC:75990-007-10 1000 mL in 1 CARTRIDGE 10 NDC:75990-007-11 1000 mL in 1 BOTTLE, PLASTIC 11 NDC:75990-007-12 1000 mL in 1 BAG 12 NDC:75990-007-13 800 mL in 1 BAG 13 NDC:75990-007-14 3785 mL in 1 BOTTLE, PLASTIC 14 NDC:75990-007-15 946 mL in 1 BOTTLE, PLASTIC 15 NDC:75990-007-28 149 mL in 1 BOTTLE, PLASTIC 16 NDC:75990-007-27 800 mL in 1 CARTRIDGE 17 NDC:75990-007-55 208200 mL in 1 DRUM 18 NDC:75990-007-08 1 in 1 BOX 18 1000 mL in 1 BAG 19 NDC:75990-007-16 236 mL in 1 BOTTLE, PLASTIC 20 NDC:75990-007-18 50 mL in 1 BOTTLE, PLASTIC 21 NDC:75990-007-17 532 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/25/2011 Labeler - Certus Medical, Inc. (966433653) Registrant - ABC Compounding Co., Inc. (003284353) Establishment Name Address ID/FEI Business Operations ABC Compounding Co., Inc. 003284353 manufacture
