FDA.reportPublic FDA data

Aquax Repellent

Product NDC
82160-252
11-digit product format
821600252
Labeler code
82160
Product ID
82160-252_d39168cb-bae3-521a-e053-2a95a90a95a5
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl Butylacetylaminopropionate
Dosage form
CREAM
Route
TOPICAL
Labeler
Pella Pharmaceuticals Co. Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2010-10-04
Marketing end
0000-00-00
Substance
ETHYL BUTYLACETYLAMINOPROPIONATE
Active strength
7500 mg/75g
NDC exclude flag
No
Listing certified through
2022-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct82160-252IInactivated by FDA2026-07-31
excluded packagepackage82160-25282160-252-01IInactivated by FDA2026-07-31

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82160-252-01Aquax Repellent75 g in 1 TUBECREAM75252
82160-252-01Aquax Repellent1 in 1 CARTONCREAM1252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82160-252AQUAX REPELLENT (ETHYL BUTYLACETYLAMINOPROPIONATE) CREAM [PELLA PHARMACEUTICALS CO. LTD]252Legacy NDC, 2 package rows20211130_d19aeb75-ce56-33ba-e053-2a95a90a5754.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82160-252-01821600252011 TUBE in 1 CARTON (82160-252-01) > 75 g in 1 TUBE1 tube2010-10-040000-00-00NoNoCurrent