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Data / Drug companies / Prestige Brands Holdings, Inc.

Prestige Brands Holdings, Inc.: 20 products in the FDA NDC directory, labeler code 67172

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

Prestige Brands Holdings, Inc. (labeler code 67172) lists 20 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 20 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on June 20, 2026.

The request: Watch Prestige Brands Holdings, Inc. (FDA labeler code 67172): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
67172
Products in commercial distribution
20
Packages
22
Finished drugs by generic name
10
Prescription products
0
Over the counter products
20
Flagged as original packager
13 of 13 products that carry the flag
Started marketing in the last 12 months
1
Products with a marketing end date set
1
Earliest marketing start
August 1, 2010
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 drugs20100%

Products by type

TypeProductsShare
Over the counter drugs20100%

Drugs it lists

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

DrugProductsCompanies listing it
Phenol531
Menthol and benzocaine41
Menthol and benzocaine and dextromethorphan hydrobromide21
Naphazoline hydrochloride and glycerin23
Acetaminophen and diphenhydramine hydrochloride129
Polyvinyl alcohol and povidone12
Glycerin and naphazoline hydrochloride12
Phenol and glycerin12
Glycerin and naphazoline hydrochloride and zinc sulfate11
Benzocaine1110

Dosage forms

Dosage formProductsShare
Lozenge735%
Spray630%
Liquid630%
Powder, for solution15%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Chloraseptic Nighttime Sore Throat Hot Relief67172-150Powder, for solutionOver the counter monograph drugsJune 20, 2026
Chloraseptic Childrens Sore Throat Cherry67172-930SprayOver the counter monograph drugsJune 20, 2024
Clear Eyes Natural Tears67172-557LiquidOver the counter monograph drugsMay 15, 2013
Chloraseptic Warming Sore Throat67172-212SprayOver the counter monograph drugsJuly 1, 2012
Chloraseptic Warming Sore Throat67172-017LozengeOver the counter monograph drugsJanuary 1, 2012
Clear Eyes Redness Relief67172-797LiquidOver the counter monograph drugsApril 27, 2011
Clear Eyes Maximum Itchy Eye Relief67172-999LiquidOver the counter monograph drugsMarch 15, 2011
Clear Eyes Triple Relief67172-898LiquidOver the counter monograph drugsMarch 15, 2011
Clear Eyes Cooling Redness Relief67172-393LiquidOver the counter monograph drugsFebruary 15, 2011
Chloraseptic Sore Throat Max67172-937SprayOver the counter monograph drugsFebruary 1, 2011
Clear Eyes Maximum Redness Relief67172-696LiquidOver the counter monograph drugsSeptember 1, 2010
Chloraseptic Sore Throat Menthol67172-113SprayOver the counter monograph drugsSeptember 1, 2010
Chloraseptic Sore Throat Citrus67172-112SprayOver the counter monograph drugsSeptember 1, 2010
Chloraseptic Sore Throat Cherry67172-111SprayOver the counter monograph drugsSeptember 1, 2010
Chloraseptic max67172-114LozengeOver the counter monograph drugsAugust 1, 2010
Chloraspetic67172-023LozengeOver the counter monograph drugsAugust 1, 2010
Chloraseptic67172-022LozengeOver the counter monograph drugsAugust 1, 2010
Chloraseptic67172-021LozengeOver the counter monograph drugsAugust 1, 2010
Chloraseptic Total Sore Throat and Cough67172-016LozengeOver the counter monograph drugsAugust 1, 2010
Chloraseptic Total Sore Throat and Cough, Sugar Free67172-015LozengeOver the counter monograph drugsAugust 1, 2010

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.