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Data / Drug companies / O&m Halyard, Inc.

O&m Halyard, Inc.: 34 products in the FDA NDC directory, labeler code 39892

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

O&m Halyard, Inc. (labeler code 39892) lists 34 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 34 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 31, 2024.

The request: Watch O&m Halyard, Inc. (FDA labeler code 39892): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
39892
Products in commercial distribution
34
Packages
55
Finished drugs by generic name
12
Prescription products
0
Over the counter products
34
Flagged as original packager
32 of 32 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
September 20, 2012
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 drugs3294.1%
New drug applications (NDA)25.9%

Products by type

TypeProductsShare
Over the counter drugs34100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Solution823.5%
Cloth720.6%
Swab720.6%
Gel38.8%
Liquid38.8%
Ointment38.8%
Paste, dentifrice25.9%
Cream12.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Halyard Chlorhexidine Gluconate39892-0961SolutionNew drug applications (NDA)July 31, 2024
Halyard Chlorhexidine Gluconate39892-0960SolutionNew drug applications (NDA)July 31, 2024
MediChoice Barrier39892-0951ClothOver the counter monograph drugsJanuary 25, 2024
MediChoice Barrier39892-0950ClothOver the counter monograph drugsJanuary 25, 2024
MediChoice PVP Scrub39892-0850SolutionOver the counter monograph drugsJanuary 25, 2024
MediChoice PVP Prep39892-0842SolutionOver the counter monograph drugsJanuary 25, 2024
MediChoice PVP Prep Solution39892-0841SolutionOver the counter monograph drugsJanuary 25, 2024
MediChoice PVP Prep39892-0840SolutionOver the counter monograph drugsJanuary 25, 2024
MediChoice Alcohol Prep Pads39892-0101ClothOver the counter monograph drugsSeptember 13, 2019
MediChoice of Hydrogen Peroxide 3 10 Volume39892-0700LiquidOver the counter monograph drugsMarch 20, 2019
MediChoice Isopropyl Rubbing Alcohol39892-0500LiquidOver the counter monograph drugsMarch 20, 2019
MediChoice Povidone-Iodine39892-0820OintmentOver the counter monograph drugsMarch 4, 2019
MediChoice Povidone-Iodine Prep Pad39892-0808ClothOver the counter monograph drugsMarch 4, 2019
Povidone-Iodine Prep39892-0809SolutionOver the counter monograph drugsMarch 1, 2019
Hydrogen Peroxide39892-0710LiquidOver the counter monograph drugsMarch 1, 2019
Antiseptic Hand Rub39892-0412GelOver the counter monograph drugsMarch 1, 2019
MediChoice Instant Hand Sanitizer Fragrance free39892-0401GelOver the counter monograph drugsJanuary 21, 2019
MediChoice Instant Hand Sanitizer Honey scented39892-0400GelOver the counter monograph drugsJanuary 21, 2019
MediChoice Alcohol Swabstick39892-0801SwabOver the counter monograph drugsJune 8, 2018
MediChoice PVP39892-0812SwabOver the counter monograph drugsAugust 29, 2017
MediChoice PVP39892-0811SwabOver the counter monograph drugsAugust 29, 2017
MediChoice OB Cleansing39892-0306ClothOver the counter monograph drugsAugust 29, 2017
MediChoice Cleansing39892-0305ClothOver the counter monograph drugsAugust 29, 2017
MediChoice BZK Antiseptic39892-0304ClothOver the counter monograph drugsAugust 29, 2017
Roll-On Antiperspirant Deodorant - Scented39892-0807SolutionOver the counter monograph drugsSeptember 24, 2015

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.