Current NDC auxiliary source row compounder:440

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: 72934-1436
Product Ndc: 72934-1436
Product Ndc Digits: 729341436
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Nendrux Gel
Proprietary Name Suffix: [empty]
Nonproprietary Name: 221034 LIDOCAINE 5% / SALICYLIC ACID 40%
Dosage Form Name: GEL
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: SALICYLIC ACID; LIDOCAINE
Active Ingredients Info: 40 g/100 mL; 5 g/100 mL
History Active Ingredients Raw: SALICYLIC ACID; LIDOCAINE
History Active Ingredients Info Raw: 40 g/100 mL; 5 g/100 mL
History Dosage Raw: GEL
Dea Schedule: [empty]
Package Ndc Raw: 72934-1436-2
Package Ndc: 72934-1436-2
Package Ndc Digits: 7293414362
Package Ndc11: 72934143602
Package Description: 30 mL in 1 BOTTLE, PUMP (72934-1436-2)
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:440
Source Row Number: 440
Source Row Hash: ba39c1ccd369d94a882d4d0d839119ceaf42242a1b880244e8868029ad5e5b03
Import Run Id: 20261017T224343Z
Loaded At: 2026-10-17 22:48:57

Exact raw FDA source fields#

{
    "ROUTENAME": "TOPICAL",
    "PRODUCTNDC": "72934-1436",
    "DEASCHEDULE": "",
    "LABELERNAME": "SKNV",
    "SUBSTANCENAME": "SALICYLIC ACID; LIDOCAINE",
    "DOSAGEFORMNAME": "GEL",
    "NDCPACKAGECODE": "72934-1436-2",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Nendrux Gel",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "221034 LIDOCAINE 5% / SALICYLIC ACID 40%",
    "PACKAGEDESCRIPTION": "30 mL in 1 BOTTLE, PUMP (72934-1436-2) ",
    "ACTIVEINGREDIENTSINFO": "40 g/100 mL; 5 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:440
Source Row Number: 440
Status Scope: package
Lookup Ndc: 72934-1436-2
Lookup Ndc Digits: 7293414362
Product Ndc: 72934-1436
Product Ndc Digits: 729341436
Package Ndc: 72934-1436-2
Package Ndc Digits: 7293414362
Package Ndc11: 72934143602
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: ba39c1ccd369d94a882d4d0d839119ceaf42242a1b880244e8868029ad5e5b03
Import Run Id: 20261017T224343Z
Loaded At: 2026-10-17 22:48:57