Home NDC 60648-7200 Companion
Product NDC 60648-7200
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 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 60648-7200-2 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 60648-7200-1 D Discontinued by firm d630ba8d3edf…732f749b63fb…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 60648-7200-1 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 60648-7200-2 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 60648-7200-1 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 60648-7200-2 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 60648-7200-1 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 60648-7200-2 I Inactivated by FDA bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60648-7200 COMPANION (COMPANION ANTIBACTERIAL HAND SOAP) LIQUID [PRESERVE INTERNATIONAL] 4 Legacy NDC 20241218_f60ebf07-ba25-45f6-a381-e4d439dab0f9.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 60648-7200-1 60648720001 .75 L in 1 BOTTLE, DISPENSING (60648-7200-1) 2020-11-04 0000-00-00 No No Current 60648-7200-2 60648720002 3.78 L in 1 BOTTLE, PLASTIC (60648-7200-2) 3.78 l 2020-11-04 0000-00-00 No No Current