FDA.reportPublic FDA data

NDC 82652-024 - Diphen

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
82652-024
Package NDCs from labels
82652-024-01
Manufacturer
Remedy Pack LLC | Safetec of America, Inc | Allegiant Health | LNK International Inc. | Granules India Limited | Ohm Laboratories
Effective date
2022-07-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DiphenRemedy Pack LLC | Safetec of America, Inc | Allegiant Health | LNK International Inc. | Granules India Limited | Ohm Laboratories2022-07-11HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82652-024-01Diphen2 in 1 PACKETTABLET, FILM COATED8200 mg1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82652-024DIPHEN (BENZOCAINE, BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, CALCIUM CARBONATE, IBUPROFEN, LORATADINE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, DIPHENHYDRAMINE HYDROCHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM OXIDE, MECLIZINE HYDROCHLORIDE, AND BISMUTH SUBSALICYLATE) KIT [REMEDY PACK LLC]1Unmatched20220717_5d185f23-8af6-4e36-b514-5662986520a5.zip