Is June Jacobs Labs LLC FDA approved?

June Jacobs Labs LLC holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are June Jacobs Labs LLC's drugs manufactured?

The FDA register lists Moonachie, NJ. Registered operations: labelling, finished drug manufacture, packaging.

What drugs does June Jacobs Labs LLC make?

7 products are listed under June Jacobs Labs LLC in the openFDA NDC Directory, most often as cream; paste; swab. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

June Jacobs Labs LLC

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

Request a quote Claim this profile

Registered sites: 1
Active NDC listings: 7
Labeller names: 2
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
June Jacobs Labs, LLCRegistrant: June Jacobs Labs LLC	46 Graphic Place, Moonachie, New Jersey (NJ) 07074-1106, United States (USA)	Labelling, Finished drug manufacture, Packaging	3002832995122610681

Catalogue

Drug listings by form and route

7 active NDC listings: 7 human otc drug. By marketing category: OTC MONOGRAPH DRUG 7.

Dosage form	NDCs
cream	3
paste	3
swab	1

Route	NDCs
topical	7

Labeller name on the listing	NDCs
june jacobs labs, llc	5
june jacobs labs llc	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Advanced Sun Resistance SPF 30	Homosalate, Octinoxate, Oxybenzone, Octisalate, Avobenzone	cream, topical	65278-319OTC MONOGRAPH DRUG
Anti-Aging Blemish Control Peel Pads	Salicylic Acid	swab, topical	65278-318OTC MONOGRAPH DRUG
Intensive Age Defying Hydrating Complex SPF 25	Homosalate, Octinoxate, Oxybenzone, Avobenzone	cream, topical	65278-103OTC MONOGRAPH DRUG
Lip Renewal SPF 50	Avobenzone, Homosalate, Octinoxate, Octisalate	paste, topical	65278-105OTC MONOGRAPH DRUG
Mineral Sun Defense Moisturizer Broad Spectrum Sunscreen SPF 30	Titanium Dioxide, Zinc Oxide	paste, topical	65278-619OTC MONOGRAPH DRUG
Protective Tinted Moisturizer Broad Spectrum Sunscreen SPF 30	Titanium Dioxide, Zinc Oxide	paste, topical	65278-104OTC MONOGRAPH DRUG
Rapid Repair Healing Cream	Allantoin, Dimethicone	cream, topical	65278-110OTC MONOGRAPH DRUG

Compare

Comparable companies in United States

Hahnemann Laboratories, Inc. dba Alpine Pharmaceuticals1 site · 4,853 NDC
NuCare Pharmaceuticals,Inc.1 site · 1,393 NDC
Greer Laboratories, Inc.1 site · 1,328 NDC
ASCLEMED USA INC. DBA ENOVACHEM1 site · 789 NDC
Golden State Medical Supply Inc.1 site · 670 NDC
Rising Pharma Holdings, Inc.1 site · 532 NDC
HF Acquisition Co LLC1 site · 363 NDC
ANI Pharmaceuticals, Inc.1 site · 299 NDC
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.1 site · 273 NDC
Newton Laboratories, Inc.1 site · 271 NDC

Enquiry

Common questions

Is June Jacobs Labs LLC FDA approved?: June Jacobs Labs LLC holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are June Jacobs Labs LLC's drugs manufactured?: The FDA register lists Moonachie, NJ. Registered operations: labelling, finished drug manufacture, packaging.
What drugs does June Jacobs Labs LLC make?: 7 products are listed under June Jacobs Labs LLC in the openFDA NDC Directory, most often as cream; paste; swab. 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.