NDC 81238-5300

aramark Antiseptic

Benzalkonium Chloride, Benzocaine

aramark Antiseptic is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Western First Aid Safety Dba Aramark. The primary component is Benzalkonium Chloride; Benzocaine.

Product ID81238-5300_47541f74-f1b1-43d1-908c-256117a8bdf5
NDC81238-5300
Product TypeHuman Otc Drug
Proprietary Namearamark Antiseptic
Generic NameBenzalkonium Chloride, Benzocaine
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2021-05-24
Marketing CategoryOTC MONOGRAPH NOT FINAL /
Application Numberpart333A
Labeler NameWestern First Aid Safety DBA Aramark
Substance NameBENZALKONIUM CHLORIDE; BENZOCAINE
Active Ingredient Strength1 mg/mL; mg/mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 81238-5300-1

59.1 mL in 1 BOTTLE, SPRAY (81238-5300-1)
Marketing Start Date2021-05-24
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "aramark Antiseptic" or generic name "Benzalkonium Chloride, Benzocaine"

NDCBrand NameGeneric Name
81238-5300aramark AntisepticBENZALKONIUM CHLORIDE, BENZOCAINE
51532-5300Antisepticbenzalkonium chloride, benzocaine
51532-5301Antisepticbenzalkonium chloride, benzocaine
61010-5300Antisepticbenzalkonium chloride, benzocaine
69103-5300Antisepticbenzalkonium chloride, benzocaine
73598-0681Antisepticbenzalkonium chloride, benzocaine
51532-4616CUT CLEANERBENZALKONIUM CHLORIDE, BENZOCAINE
81238-4616CUT CLEANERBENZALKONIUM CHLORIDE, BENZOCAINE
50332-0212First AidBenzalkonium Chloride, Benzocaine
62985-5081First Aid Antisepticbenzalkonium chloride, benzocaine
0498-0015North First Aid AntisepticBenzalkonium Chloride, Benzocaine
10237-798Orajel Cold Sore Touch Free - Single DoseBenzalkonium Chloride, Benzocaine
10237-741Orajel for Cold SoresBenzalkonium Chloride, Benzocaine
10237-756Orajel for Cold SoresBenzalkonium Chloride, Benzocaine
67659-150Orajel for Cold SoresBenzalkonium Chloride, Benzocaine

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.