Current NDC auxiliary source row compounder:136

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: 72934-4601
Product Ndc: 72934-4601
Product Ndc Digits: 729344601
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Hentis
Proprietary Name Suffix: [empty]
Nonproprietary Name: 031030 MINOXIDIL 5% / PROGESTERONE 0.1% / TRETINOIN 0.025%
Dosage Form Name: SOLUTION
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: TRETINOIN; MINOXIDIL; PROGESTERONE
Active Ingredients Info: .025 g/100 mL; 5 g/100 mL; .1 g/100 mL
History Active Ingredients Raw: TRETINOIN; MINOXIDIL; PROGESTERONE
History Active Ingredients Info Raw: .025 g/100 mL; 5 g/100 mL; .1 g/100 mL
History Dosage Raw: SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 72934-4601-8
Package Ndc: 72934-4601-8
Package Ndc Digits: 7293446018
Package Ndc11: 72934460108
Package Description: 60 mL in 1 BOTTLE, GLASS (72934-4601-8)
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:136
Source Row Number: 136
Source Row Hash: d83f5200be30a92f32447f5d7fedddcf1444a3e0401d7dbaf1fca911e0891ca0
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09

Exact raw FDA source fields#

{
    "ROUTENAME": "TOPICAL",
    "PRODUCTNDC": "72934-4601",
    "DEASCHEDULE": "",
    "LABELERNAME": "SKNV",
    "SUBSTANCENAME": "TRETINOIN; MINOXIDIL; PROGESTERONE",
    "DOSAGEFORMNAME": "SOLUTION",
    "NDCPACKAGECODE": "72934-4601-8",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Hentis",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "031030 MINOXIDIL 5% / PROGESTERONE 0.1% / TRETINOIN 0.025%",
    "PACKAGEDESCRIPTION": "60 mL in 1 BOTTLE, GLASS (72934-4601-8) ",
    "ACTIVEINGREDIENTSINFO": ".025 g/100 mL; 5 g/100 mL; .1 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:136
Source Row Number: 136
Status Scope: package
Lookup Ndc: 72934-4601-8
Lookup Ndc Digits: 7293446018
Product Ndc: 72934-4601
Product Ndc Digits: 729344601
Package Ndc: 72934-4601-8
Package Ndc Digits: 7293446018
Package Ndc11: 72934460108
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: d83f5200be30a92f32447f5d7fedddcf1444a3e0401d7dbaf1fca911e0891ca0
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09