Current NDC auxiliary source row compounder:75

This page is keyed by dataset, FDA.report source record ID, and physical source row number. Empty values are shown rather than omitted.

Complete normalized row#

Record Source: ndc_compounder_zip
Product Ndc Raw: 72934-6394
Product Ndc: 72934-6394
Product Ndc Digits: 729346394
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Keya Emulsion
Proprietary Name Suffix: [empty]
Nonproprietary Name: 141074 HYDROCORTISONE 0.5% / HYDROQUINONE 6%
Dosage Form Name: EMULSION
Route Name: TOPICAL
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: SKNV
Establishment Name: SKNV
Establishment Fei: [empty]
Substance Name: HYDROCORTISONE; HYDROQUINONE
Active Ingredients Info: .5 g/100 mL; 6 g/100 mL
History Active Ingredients Raw: HYDROCORTISONE; HYDROQUINONE
History Active Ingredients Info Raw: .5 g/100 mL; 6 g/100 mL
History Dosage Raw: EMULSION
Dea Schedule: [empty]
Package Ndc Raw: 72934-6394-2
Package Ndc: 72934-6394-2
Package Ndc Digits: 7293463942
Package Ndc11: 72934639402
Package Description: 30 mL in 1 BOTTLE, PUMP (72934-6394-2)
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
Normalization Status: valid
Source Url: https://www.accessdata.fda.gov/cder/compounders_ndc_directory.zip
Source Archive: compounders_ndc_directory.zip
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Last Modified: Fri, 18 Sep 2026 15:17:23 GMT
Source Archive Sha256: 222f6800f79cb1a0fa79431b7226bd6b34899999dbf086af51004a96774ada98
Source Member Sha256: f8d9743e5616579a34d614887e86a53913efa0a63d3138d59d2f87cbb4d0cc17
Source Record Id: compounder:75
Source Row Number: 75
Source Row Hash: 7f4addba871078fc1c495d001da703825f7ea8aded760f1aeb7f0ce545f40b9c
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09

Exact raw FDA source fields#

{
    "ROUTENAME": "TOPICAL",
    "PRODUCTNDC": "72934-6394",
    "DEASCHEDULE": "",
    "LABELERNAME": "SKNV",
    "SUBSTANCENAME": "HYDROCORTISONE; HYDROQUINONE",
    "DOSAGEFORMNAME": "EMULSION",
    "NDCPACKAGECODE": "72934-6394-2",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Keya Emulsion",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "141074 HYDROCORTISONE 0.5% / HYDROQUINONE 6%",
    "PACKAGEDESCRIPTION": "30 mL in 1 BOTTLE, PUMP (72934-6394-2) ",
    "ACTIVEINGREDIENTSINFO": ".5 g/100 mL; 6 g/100 mL",
    "MARKETINGCATEGORYNAME": "OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)",
    "PROPRIETARYNAMESUFFIX": ""
}

Normalization notes#

[]

Current status projection#

Dataset: compounder
Record Source: ndc_compounder_zip
Source Record Id: compounder:75
Source Row Number: 75
Status Scope: package
Lookup Ndc: 72934-6394-2
Lookup Ndc Digits: 7293463942
Product Ndc: 72934-6394
Product Ndc Digits: 729346394
Package Ndc: 72934-6394-2
Package Ndc Digits: 7293463942
Package Ndc11: 72934639402
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 7f4addba871078fc1c495d001da703825f7ea8aded760f1aeb7f0ce545f40b9c
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09