NDC 24730-801 - Excel

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
24730-801
Package NDCs from labels
24730-801-09, 24730-801-08
Manufacturer
United Pet Group | JUNGLE LABORATORIES CORPORATION
Effective date
2010-04-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Excel - United Pet Group | JUNGLE LABORATORIES CORPORATIONUnited Pet Group | JUNGLE LABORATORIES CORPORATION2010-04-06OTC ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HydrocortisoneACTIVE INGREDIENTWI4X0X7BPJEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
HydrocortisoneACTIVE MOIETYWI4X0X7BPJEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
DIAZOLIDINYL UREAINACTIVE INGREDIENTH5RIZ3MPW4EXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
GLYCERININACTIVE INGREDIENTPDC6A3C0OXEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
GLYCERYL MONOSTEARATEINACTIVE INGREDIENT230OU9XXE4EXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
ISOPROPYL MYRISTATEINACTIVE INGREDIENT0RE8K4LNJSEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YHEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3EXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JEXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4
WATERINACTIVE INGREDIENT059QF0KO0REXCEL (HYDROCORTISONE) SALVE [UNITED PET GROUP]4

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 53 of 53 · 1,047 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AdditoxTRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, PHYTOLACCA DECANDRA, ARSENICUM ALBUM, BELLADONNA, CHELIDONIUM MAJUS, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUMBioActive Nutritional, Inc.319ee2fe-58e3-495e-bf0d-df201f6fbb1c2018-07-18WarningsExact identifier
unii: Z8IX2SC1OH
unii: A2I8C7HI9T
Intensive Healing EczemaHYDROCORTISONEWalgreens3d27f041-c554-4139-87b5-709537785f222018-02-04WarningsExact identifier
unii: WI4X0X7BPJ
Homeoplex DGLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,Supplement Clinic, LLC.cd6b48ab-3566-484d-8deb-15ef6f8e7e8f2017-11-01WarningsExact identifier
unii: PDC6A3C0OX
Sterile WaterWATERBaxter Healthcare Corporationef3e79c5-3f58-4b36-a296-64b7d9a651c12017-10-17Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
FIND BICHON CLEANSING MASKGLYCERINPioom Cosmetic Co.,ltd50b7db48-7b55-6df4-e054-00144ff88e882017-05-30WarningsExact identifier
unii: PDC6A3C0OX
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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