FDA.reportPublic FDA data

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Product NDC
74487-101
Requested package NDC
74487-101-13
11-digit product format
744870101
Labeler code
74487
Product ID
74487-101_b1d1c7de-8b76-4eeb-92df-d246e6b2ce07
Type
HUMAN OTC DRUG
Nonproprietary name
ETHYL ALCOHOL
Dosage form
SOLUTION
Route
TOPICAL
Labeler
GREENERWAYS LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-04-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage74487-10174487-101-13DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
74487-101-1374487010113100 mL in 1 BOTTLE (74487-101-13) 100 ml2020-04-030000-00-00NoNoCurrent