NDC 52380-1272

Aplicare Antiseptic Chlorhexidine Gluconate

Chlorhexidine Gluconate

Aplicare Antiseptic Chlorhexidine Gluconate is a Topical Solution in the Human Otc Drug category. It is labeled and distributed by Aplicare, Inc.. The primary component is Chlorhexidine Gluconate.

Product ID52380-1272_1d107814-357c-68e4-e054-00144ff88e88
NDC52380-1272
Product TypeHuman Otc Drug
Proprietary NameAplicare Antiseptic Chlorhexidine Gluconate
Generic NameChlorhexidine Gluconate
Dosage FormSolution
Route of AdministrationTOPICAL
Marketing Start Date1998-09-01
Marketing CategoryNDA / NDA
Application NumberNDA019125
Labeler NameAplicare, Inc.
Substance NameCHLORHEXIDINE GLUCONATE
Active Ingredient Strength4 g/100mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 52380-1272-4

118 mL in 1 BOTTLE (52380-1272-4)
Marketing Start Date1998-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52380-1272-7 [52380127207]

Aplicare Antiseptic Chlorhexidine Gluconate SOLUTION
Marketing CategoryNDA
Application NumberNDA019125
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date1998-09-01
Inactivation Date2020-01-31

NDC 52380-1272-4 [52380127204]

Aplicare Antiseptic Chlorhexidine Gluconate SOLUTION
Marketing CategoryNDA
Application NumberNDA019125
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date1998-09-01
Inactivation Date2020-01-31

NDC 52380-1272-6 [52380127206]

Aplicare Antiseptic Chlorhexidine Gluconate SOLUTION
Marketing CategoryNDA
Application NumberNDA019125
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date1998-09-01
Inactivation Date2020-01-31

NDC 52380-1272-8 [52380127208]

Aplicare Antiseptic Chlorhexidine Gluconate SOLUTION
Marketing CategoryNDA
Application NumberNDA019125
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date1998-09-01
Inactivation Date2020-01-31

NDC 52380-1272-9 [52380127209]

Aplicare Antiseptic Chlorhexidine Gluconate SOLUTION
Marketing CategoryNDA
Application NumberNDA019125
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date1998-09-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CHLORHEXIDINE GLUCONATE4 g/100mL

OpenFDA Data

SPL SET ID:45c1e1b3-6d56-4fa2-a332-4e88d2f416dc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 211365
  • NDC Crossover Matching brand name "Aplicare Antiseptic Chlorhexidine Gluconate" or generic name "Chlorhexidine Gluconate"

    NDCBrand NameGeneric Name
    0116-1272Aplicare Antiseptic Chlorhexidine GluconateChlorhexidine Gluconate
    52380-1274Aplicare Antiseptic Chlorhexidine GluconateAplicare Antiseptic Chlorhexidine Gluconate
    52380-1272Aplicare Antiseptic Chlorhexidine GluconateAplicare Antiseptic Chlorhexidine Gluconate
    52380-1987Aplicare Antiseptic Chlorhexidine GluconateAplicare Antiseptic Chlorhexidine Gluconate
    52380-1986Aplicare Antiseptic Chlorhexidine GluconateAplicare Antiseptic Chlorhexidine Gluconate
    0116-0407ANTISEPTIC SKIN CLEANSERCHLORHEXIDINE GLUCONATE
    0116-1061ANTISEPTIC SKIN CLEANSERChlorhexidine Gluconate
    0116-2800Antiseptic Skin CleanserCHLORHEXIDINE GLUCONATE
    0116-1919Aplicare Chlorhexidine Gluconate 2% SolutionChlorhexidine Gluconate
    0116-1322Bactoshield CHGChlorhexidine Gluconate
    0116-1344Bactoshield CHGCHLORHEXIDINE GLUCONATE
    0116-0505BD E-Z Scrubchlorhexidine gluconate
    0116-0506BD E-Z Scrubchlorhexidine gluconate
    0116-0101Chlorhexidine GluconateChlorhexidine Gluconate
    0116-0175Chlorhexidine GluconateChlorhexidine Gluconate
    0116-0301Chlorhexidine GluconateChlorhexidine Gluconate
    0116-2001Chlorhexidine GluconateChlorhexidine Gluconate
    0116-0003Chlorhexidine Gluconate 0.12% Oral RinseCHLORHEXIDINE GLUCONATE
    0116-1021DYNA-HEXChlorhexidine gluconate
    0116-1060DYNA-HEX 4Chlorhexidine Gluconate
    0116-0800NUPRO Chlorhexidine GluconateCHLORHEXIDINE GLUCONATE
    0116-0620Peridexchlorhexidine gluconate
    0116-0722Scrub CareCHLORHEXIDINE GLUCONATE
    0116-2992Scrub CareCHLORHEXIDINE GLUCONATE

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.