NDC 27426-050-25 - Keratex KHS

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: 27426-050
Requested NDC: 27426-050-25
Package NDCs from labels: 27426-050-25
Manufacturer: Penleigh Irving Ltd
Effective date: 2018-12-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Keratex KHS - Penleigh Irving Ltd	Penleigh Irving Ltd	2018-12-20	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
27426-050-25	KeratexKHS	250 mL in 1 BOTTLE, PLASTIC	LIQUID	250		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
27426-050	KERATEX KHS (BUTYL ACETATE, DIETHYLHEXYL SEBACATE AND PYROXYLIN) LIQUID [PENLEIGH IRVING LTD]	6	1 package rows	20181221_646df2e8-986d-4f29-a41e-8ec07bc00cad.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BUTYL ACETATE	ACTIVE INGREDIENT	464P5N1905	KERATEX KHS (BUTYL ACETATE, DIETHYLHEXYL SEBACATE AND PYROXYLIN) LIQUID [PENLEIGH IRVING LTD]	5
DIETHYLHEXYL SEBACATE	ACTIVE INGREDIENT	U9LS47Q72Q	KERATEX KHS (BUTYL ACETATE, DIETHYLHEXYL SEBACATE AND PYROXYLIN) LIQUID [PENLEIGH IRVING LTD]	5
PYROXYLIN	ACTIVE INGREDIENT	KYR8BR2X6O	KERATEX KHS (BUTYL ACETATE, DIETHYLHEXYL SEBACATE AND PYROXYLIN) LIQUID [PENLEIGH IRVING LTD]	5
BUTYL ACETATE	ACTIVE MOIETY	464P5N1905	KERATEX KHS (BUTYL ACETATE, DIETHYLHEXYL SEBACATE AND PYROXYLIN) LIQUID [PENLEIGH IRVING LTD]	5
DIETHYLHEXYL SEBACATE	ACTIVE MOIETY	U9LS47Q72Q	KERATEX KHS (BUTYL ACETATE, DIETHYLHEXYL SEBACATE AND PYROXYLIN) LIQUID [PENLEIGH IRVING LTD]	5
Pyroxylin	ACTIVE MOIETY	KYR8BR2X6O	KERATEX KHS (BUTYL ACETATE, DIETHYLHEXYL SEBACATE AND PYROXYLIN) LIQUID [PENLEIGH IRVING LTD]	5

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 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Household Antigens	ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PROPYLPARABEN, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR, PARAFFINUM	Energique, Inc.	f3db63df-62a4-48d6-92e7-94e4a5701552	2024-12-20	Warnings	Exact identifier unii: 464P5N1905
Household Antigens	ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR	Energique, Inc.	87c92497-8a51-4977-87fe-e0b4c6bafb19	2024-09-27	Warnings	Exact identifier unii: 464P5N1905

Reported adverse events (FAERS/openFDA)#

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