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Data / Drug companies / JHK Inc DBA American Safety & First Aid

JHK Inc DBA American Safety & First Aid: 26 products in the FDA NDC directory, labeler code 73598

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

JHK Inc DBA American Safety & First Aid (labeler code 73598) lists 26 products in the FDA National Drug Code Directory, covering 18 finished drugs by generic name. By type: 26 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on October 11, 2024.

The request: Watch JHK Inc DBA American Safety & First Aid (FDA labeler code 73598): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
73598
Products in commercial distribution
26
Packages
27
Finished drugs by generic name
18
Prescription products
0
Over the counter products
26
Flagged as original packager
24 of 24 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
2
Earliest marketing start
February 2, 2000
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs2388.5%
Generic drugs (ANDA)27.7%
Unapproved homeopathic products13.8%

Products by type

TypeProductsShare
Over the counter drugs26100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Tablet726.9%
Spray415.4%
Tablet, chewable415.4%
Capsule, coated415.4%
Lozenge311.5%
Tablet, coated27.7%
Cream13.8%
Ointment13.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Citrus Flavored Antacid73598-1392Tablet, chewableOver the counter monograph drugsOctober 11, 2024
Cramp Tabs73598-1472Capsule, coatedOver the counter monograph drugsJune 26, 2024
Maximum Strength Cold Tabs73598-1342Capsule, coatedOver the counter monograph drugsJune 26, 2024
Maximum Strength Backache Relief73598-1272Capsule, coatedOver the counter monograph drugsJune 26, 2024
Pain and Sinus Reliever73598-1194TabletOver the counter monograph drugsMay 9, 2024
Pain and Sinus73598-1192TabletOver the counter monograph drugsMay 9, 2024
Antiseptic73598-0681SprayOver the counter monograph drugsFebruary 14, 2020
Burn73598-0671SprayOver the counter monograph drugsFebruary 14, 2020
Hydrogen Peroxide73598-0661SprayOver the counter monograph drugsFebruary 14, 2020
Isopropyl Alcohol73598-0651SprayOver the counter monograph drugsFebruary 14, 2020
Extra Strength Pain Reliever73598-1372Capsule, coatedOver the counter monograph drugsFebruary 2, 2000
NASAL and SINUS DECONGESTANT73598-1264TabletOver the counter monograph drugsFebruary 2, 2000
NASAL and SINUS DECONGESTANT73598-1262TabletOver the counter monograph drugsFebruary 2, 2000
Cold eeze73598-1242LozengeUnapproved homeopathic productsFebruary 2, 2000
Pept-ache73598-1232Tablet, chewableOver the counter monograph drugsFebruary 2, 2000
Cherry cough drops 100ct73598-1204LozengeOver the counter monograph drugsFebruary 2, 2000
Cherry cough drops 50ct73598-1202LozengeOver the counter monograph drugsFebruary 2, 2000
Mint antacid 25073598-1144Tablet, chewableOver the counter monograph drugsFebruary 2, 2000
Mint antacid 10073598-1142Tablet, chewableOver the counter monograph drugsFebruary 2, 2000
Maximum strength non-aspirin 25073598-1124TabletOver the counter monograph drugsFebruary 2, 2000
Maximum strength non-aspirin 10073598-1122TabletOver the counter monograph drugsFebruary 2, 2000
Aspirin 50 CT73598-1112TabletOver the counter monograph drugsFebruary 2, 2000
Ibuprofen 25073598-1104Tablet, coatedGeneric drugs (ANDA)February 2, 2000
Ibuprofen 10073598-1102Tablet, coatedGeneric drugs (ANDA)February 2, 2000
Hydrocortisone73598-1014CreamOver the counter monograph drugsFebruary 2, 2000

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.