Antibacterial hand and skin wet wipe

Product NDC
79781-205
11-digit product format
797810205
Labeler code
79781
Product ID
79781-205_a9db2b69-81fb-1adb-e053-2995a90aba0b
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
SWAB
Route
TOPICAL
Labeler
MOLECULE KORUYUCU SAGLIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-07-23
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79781-205-012022-09-16C16284748780-1d6a99b39-acc3-a426-e053-dadaa90af4c2a9db2b69-81fa-1adb-e053-2995a90aba0b
79781-205-012022-01-28C16284748780-1d6a99b39-acc3-a426-e053-dadaa90af4c2a9db2b69-81fa-1adb-e053-2995a90aba0b

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79781-205-01797810205015.1 g in 1 PACKAGE (79781-205-01) 5.1 g2020-07-230000-00-00NoNoCurrent