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Recens Foam (Certus Medical, Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 1200 mL in 1 CARTRIDGE (75990-968-01) Label Information
LIQUID 700 mL in 1 BAG (75990-968-07) Label Information
LIQUID 540 mL in 1 BOTTLE, PLASTIC (75990-968-05) Label Information
LIQUID 1 BAG in 1 BOX (75990-968-06) > 800 mL in 1 BAG Label Information
LIQUID 350 mL in 1 CARTRIDGE (75990-968-03) Label Information
LIQUID 1 BAG in 1 BOX (75990-968-08) > 1000 mL in 1 BAG Label Information
LIQUID 532 mL in 1 BOTTLE, PLASTIC (75990-968-17) Label Information
LIQUID 118 mL in 1 BOTTLE, PLASTIC (75990-968-24) Label Information
LIQUID 50 mL in 1 BOTTLE, PLASTIC (75990-968-18) Label Information
LIQUID 1000 mL in 1 CARTRIDGE (75990-968-10) Label Information
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (75990-968-11) Label Information
LIQUID 800 mL in 1 CARTRIDGE (75990-968-27) Label Information
LIQUID 208200 mL in 1 DRUM (75990-968-55) Label Information
LIQUID 236 mL in 1 BOTTLE, PLASTIC (75990-968-16) Label Information
LIQUID 2000 mL in 1 CARTRIDGE (75990-968-09) Label Information
LIQUID 800 mL in 1 BAG (75990-968-13) Label Information
LIQUID 946 mL in 1 BOTTLE, PLASTIC (75990-968-15) Label Information
LIQUID 3785 mL in 1 BOTTLE, PLASTIC (75990-968-14) Label Information
LIQUID 149 mL in 1 BOTTLE, PLASTIC (75990-968-28) Label Information
LIQUID 1000 mL in 1 BAG (75990-968-12) Label Information
LIQUID 473 mL in 1 BOTTLE, PLASTIC (75990-968-30) Label Information

Complete Recens Foam Information

  • Drug Facts Box OTC-Active Ingredient Section

    Ethyl Alcohol 62% v/v


  • Drug Facts Box OTC-Purpose Section

    Antiseptic


  • Drug Facts Box OTC-Indications & Usage Section

    for hand-washing to decrease bacteria on the skin

    if hands are visibly soiled, use regular soap and water

    recommended for repeated use


  • Drug Facts Box OTC-Warnings Section

    FLAMMABLE, keep away from fire and flames

    For external use only


  • Drug Facts Box OTC-When Using Section

    do not get into eyes

    if contact occurs, rinse eyes thoroughly with water


  • Drug Facts Box OTC-Stop Use Section

    irritation and redness develop


  • Drug Facts Box OTC-Keep Out of Reach of Children Section

    if swallowed, get medical help or contact a Poison Control Center right away


  • Drug Facts Box OTC-Dosage & Administration Section

     apply to hands and rub lightly until dry without wiping or rinsing


  • Drug Facts Box OTC-Inactive Ingredient Section

    water, DEA-C8-18 perfluoroalkylethyl phosphate, propylene glycol


  • Recens Foam 6968 1000ml

    product label

    Recens Foam  1000ml  


  • INGREDIENTS AND APPEARANCE
    RECENS FOAM 
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:75990-968
    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:75990-968-30 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    2 NDC:75990-968-06 1 in 1 BOX 05/19/2011
    2 800 mL in 1 BAG; Type 0: Not a Combination Product
    3 NDC:75990-968-24 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    4 NDC:75990-968-01 1200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 05/19/2011
    5 NDC:75990-968-03 350 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 05/19/2011
    6 NDC:75990-968-05 540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    7 NDC:75990-968-07 700 mL in 1 BAG; Type 0: Not a Combination Product 05/19/2011
    8 NDC:75990-968-09 2000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 05/19/2011
    9 NDC:75990-968-10 1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 05/19/2011
    10 NDC:75990-968-11 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    11 NDC:75990-968-12 1000 mL in 1 BAG; Type 0: Not a Combination Product 05/19/2011
    12 NDC:75990-968-13 800 mL in 1 BAG; Type 0: Not a Combination Product 05/19/2011
    13 NDC:75990-968-14 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    14 NDC:75990-968-15 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    15 NDC:75990-968-28 149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    16 NDC:75990-968-27 800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product 05/19/2011
    17 NDC:75990-968-08 1 in 1 BOX 05/19/2011
    17 1000 mL in 1 BAG; Type 0: Not a Combination Product
    18 NDC:75990-968-16 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    19 NDC:75990-968-18 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    20 NDC:75990-968-17 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/19/2011
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 05/19/2011
    Labeler - Certus Medical, Inc. (966433653)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    Name Address ID/FEI Business Operations
    ABC Compounding Co., Inc. 003284353 manufacture(75990-968)