NDC 0859-2378 - ChlorhexiDerm 4%

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0859-2378
Package NDCs from labels
0859-2378-01, 0859-2378-02
Manufacturer
Bayer HealthCare LLC
Effective date
2022-10-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ChlorhexiDerm 4% - Bayer HealthCare LLCBayer HealthCare LLC2022-10-27PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CETRIMONIUM CHLORIDEACTIVE INGREDIENTUC9PE95IBPCHLORHEXIDERM 4% (CHLORHEXIDERM) SHAMPOO [BAYER HEALTHCARE LLC]1
CHLORHEXIDINE GLUCONATEACTIVE INGREDIENTMOR84MUD8ECHLORHEXIDERM 4% (CHLORHEXIDERM) SHAMPOO [BAYER HEALTHCARE LLC]1
CETRIMONIUMACTIVE MOIETYZ7FF1XKL7ACHLORHEXIDERM 4% (CHLORHEXIDERM) SHAMPOO [BAYER HEALTHCARE LLC]1
CHLORHEXIDINEACTIVE MOIETYR4KO0DY52LCHLORHEXIDERM 4% (CHLORHEXIDERM) SHAMPOO [BAYER HEALTHCARE LLC]1
4,5-DICHLORO-2-OCTYL-3-ISOTHIAZOLONEINACTIVE INGREDIENTHCY9Q844W2CHLORHEXIDERM 4% (CHLORHEXIDERM) SHAMPOO [BAYER HEALTHCARE LLC]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 9 of 9 · 162 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ANTISEPTIC SKIN CLEANSERCHLORHEXIDINE GLUCONATEXttrium Laboratories, Inc.6e62eb50-ebaa-361e-e053-2991aa0aba6f2018-06-11WarningsExact identifier
unii: MOR84MUD8E
Hand WipesCHLORHEXIDINE DIGLUCONATE AND BENZETHONIUM CHLORIDEJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.181e5fa0-ddda-4783-a0b5-ff95bfce6b362017-10-09WarningsExact identifier
unii: MOR84MUD8E

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.