Is Uline. FDA approved?

Uline. holds no registered establishment of its own; 15 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does Uline. make?

15 products are listed under Uline. in the openFDA NDC Directory, most often as tablet, film coated; liquid; gel. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Uline.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 0
Active NDC listings: 15
Labeller names: 3
Live patents: 0
Countries: 0

Catalogue

Drug listings by form and route

15 active NDC listings: 15 human otc drug. By marketing category: OTC MONOGRAPH DRUG 12, ANDA 2, NDA 1.

Dosage form	NDCs
tablet, film coated	4
liquid	3
gel	2
soap	2
solution	1
tablet	1
tablet, chewable	1
tablet, coated	1

Route	NDCs
oral	7
topical	7
ophthalmic	1

Labeller name on the listing	NDCs
uline	12
uline	2
uline.	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Alcohol	Alcohol	liquid, topical	69790-849OTC MONOGRAPH DRUG
Antibacterial	Benzalkonium chloride 0.13%	soap, topical	69790-279OTC MONOGRAPH DRUG
Antibacterial Hand Wash	Benzalkonium chloride 0.13%	liquid, topical	69790-488OTC MONOGRAPH DRUG
Hand Sanitizer	Alcohol	liquid, topical	69790-456OTC MONOGRAPH DRUG
Hand Sanitizer	Ethyl Alcohol	gel, topical	69790-770OTC MONOGRAPH DRUG
Hand Wash	Benzalkonium chloride	soap, topical	69790-466OTC MONOGRAPH DRUG
ULINE Aspirin	Aspirin	tablet, film coated, oral	69790-616OTC MONOGRAPH DRUG
ULINE Eyewash	Eyewash	solution, ophthalmic	69790-010NDA
Uline Acetaminophen Extra Strength	acetaminophen	tablet, film coated, oral	69790-154OTC MONOGRAPH DRUG
Uline Acetaminophen Extra Strength	acetaminophen	tablet, film coated, oral	69790-173OTC MONOGRAPH DRUG
Uline Acetaminophen Extra Strength	acetaminophen	tablet, film coated, oral	69790-804OTC MONOGRAPH DRUG
Uline Antacid	calcium carbonate	tablet, chewable, oral	69790-820OTC MONOGRAPH DRUG
Uline Hand Sanitizer	Alcohol	gel, topical	69790-801OTC MONOGRAPH DRUG
Uline Ibuprofen	Ibuprofen	tablet, coated, oral	69790-609ANDA
Uline Ibuprofen	Ibuprofen	tablet, oral	69790-709ANDA

Compare

Other companies listing alcohol

The Procter & Gamble Manufacturing Company11 sites · 849 NDC
Isomedix Operations Inc9 sites · 48 NDC
Ecolab Inc.6 sites · 105 NDC
Medline Industries, LP5 sites · 122 NDC
Church & Dwight Co., Inc.4 sites · 157 NDC
Nice-Pak Products, LLC4 sites · 48 NDC
United Therapeutics Corporation4 sites · 40 NDC
International Medication Systems, Ltd.3 sites · 2,801 NDC
STERIS Corporation3 sites · 1 NDC
PureTek Corporation2 sites · 178 NDC

Enquiry

Common questions

Is Uline. FDA approved?: Uline. holds no registered establishment of its own; 15 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Uline. make?: 15 products are listed under Uline. in the openFDA NDC Directory, most often as tablet, film coated; liquid; gel. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.