FDA.reportPublic FDA data

Companion

Product NDC
60648-7200
Requested package NDC
60648-7200-1
11-digit product format
606487200
Labeler code
60648
Product ID
60648-7200_ad4fd5df-d9e6-4748-94ef-b2ba6d5668c9
Type
HUMAN OTC DRUG
Nonproprietary name
Companion Antibacterial Hand Soap
Dosage form
LIQUID
Route
TOPICAL
Labeler
Preserve International
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-11-04
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
3 mg/L
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage60648-720060648-7200-1DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2022-08-30 03:57 UTC · source 2022-08-29IInactivated by FDAfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
60648-7200-12023-07-24COMPANION Foaming Antibacterial Hand Soap
60648-7200-22023-07-24COMPANION Foaming Antibacterial Hand Soap
60648-7200-12022-01-28COMPANION Foaming Antibacterial Hand Soap
60648-7200-22022-01-28COMPANION Foaming Antibacterial Hand Soap

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60648-7200COMPANION (COMPANION ANTIBACTERIAL HAND SOAP) LIQUID [PRESERVE INTERNATIONAL]4Legacy NDC20241218_f60ebf07-ba25-45f6-a381-e4d439dab0f9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
60648-7200-160648720001.75 L in 1 BOTTLE, DISPENSING (60648-7200-1) 2020-11-040000-00-00NoNoCurrent