Current NDC auxiliary source row compounder:77

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: 72934-1591
Product Ndc: 72934-1591
Product Ndc Digits: 729341591
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Aluxof
Proprietary Name Suffix: [empty]
Nonproprietary Name: 011727 BENZOYL PEROXIDE 10% / SPIRONOLACTONE 4% CLINDAMYCIN 2% / NIACINAMIDE 4% / TRETINOIN 0.05%
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: SPIRONOLACTONE; BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE; NIACINAMIDE; TRETINOIN
Active Ingredients Info: 4 g/100 g; 10 g/100 g; 2 g/100 g; 4 g/100 g; .05 g/100 g
History Active Ingredients Raw: SPIRONOLACTONE; BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE; NIACINAMIDE; TRETINOIN
History Active Ingredients Info Raw: 4 g/100 g; 10 g/100 g; 2 g/100 g; 4 g/100 g; .05 g/100 g
History Dosage Raw: GEL
Dea Schedule: [empty]
Package Ndc Raw: 72934-1591-2
Package Ndc: 72934-1591-2
Package Ndc Digits: 7293415912
Package Ndc11: 72934159102
Package Description: 30 g in 1 BOTTLE, PUMP (72934-1591-2)
Reporting Period Raw: 2026-1
Reporting Period: 2026-1
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:77
Source Row Number: 77
Source Row Hash: 81c10f496b833b6912482890c194f1ded46b2bb221d75f9d298ee14a9affad42
Import Run Id: 20261015T130142Z
Loaded At: 2026-10-15 13:06:14

Exact raw FDA source fields#

{
    "ROUTENAME": "TOPICAL",
    "PRODUCTNDC": "72934-1591",
    "DEASCHEDULE": "",
    "LABELERNAME": "SKNV",
    "SUBSTANCENAME": "SPIRONOLACTONE; BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE; NIACINAMIDE; TRETINOIN",
    "DOSAGEFORMNAME": "GEL",
    "NDCPACKAGECODE": "72934-1591-2",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Aluxof",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "011727 BENZOYL PEROXIDE 10% / SPIRONOLACTONE 4%  CLINDAMYCIN 2% / NIACINAMIDE 4% / TRETINOIN 0.05%",
    "PACKAGEDESCRIPTION": "30 g in 1 BOTTLE, PUMP (72934-1591-2) ",
    "ACTIVEINGREDIENTSINFO": "4 g/100 g; 10 g/100 g; 2 g/100 g; 4 g/100 g; .05 g/100 g",
    "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:77
Source Row Number: 77
Status Scope: package
Lookup Ndc: 72934-1591-2
Lookup Ndc Digits: 7293415912
Product Ndc: 72934-1591
Product Ndc Digits: 729341591
Package Ndc: 72934-1591-2
Package Ndc Digits: 7293415912
Package Ndc11: 72934159102
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2026-1
Reporting Period: 2026-1
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 81c10f496b833b6912482890c194f1ded46b2bb221d75f9d298ee14a9affad42
Import Run Id: 20261015T130142Z
Loaded At: 2026-10-15 13:06:14