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Data / Drug companies / Publix Super Markets Inc

Publix Super Markets Inc: 152 products in the FDA NDC directory, labeler code 56062

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

Publix Super Markets Inc (labeler code 56062) lists 152 products in the FDA National Drug Code Directory, covering 78 finished drugs by generic name. By type: 152 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 15, 2026.

The request: Watch Publix Super Markets Inc (FDA labeler code 56062): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
56062
Products in commercial distribution
152
Packages
213
Finished drugs by generic name
78
Prescription products
0
Over the counter products
152
Flagged as original packager
146 of 146 products that carry the flag
Started marketing in the last 12 months
17
Products with a marketing end date set
10
Earliest marketing start
September 15, 1988
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 drugs7650%
Generic drugs (ANDA)7146.7%
New drug applications (NDA)53.3%

Products by type

TypeProductsShare
Over the counter drugs152100%

Drugs it lists

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

DrugProductsCompanies listing it
Nicotine polacrilex2257
Ibuprofen8190
Acetaminophen6214
Aspirin5134
Sodium fluoride4124
Loratadine4125
Acetaminophen, dextromethorphan hbr, doxylamine succinate340
Famotidine3138
Naproxen sodium3100
Cetirizine hydrochloride3119
Eucalyptol, menthol, methyl salicylate, thymol342
Minoxidil2113
Magnesium citrate229
Pyrithione zinc276
Cetirizine hcl248
Diphenhydramine hcl299
Acetaminophen, dextromethorphan hbr, phenylephrine hcl245
Isopropyl alcohol2177
Diclofenac sodium2109
Bisacodyl260
Pseudoephedrine hydrochloride223
Diphenhydramine hydrochloride2127
Omeprazole2106
Loperamide hydrochloride282
Cetylpyridinium chloride247
Miconazole nitrate1101
Cetirizine hydrochloride, pseudoephedrine hydrochloride118
Docusate sodium179
Acetaminophen, aspirin and caffeine126
Ibuprofen and pseudoephedrine hydrochloride16
Doxylamine succinate139
Pronamel repair whitening11
Dimethicone169
Simethicone186
Polyvinyl alcohol, povidone118
Lidocaine hcl, menthol117
Witch hazel163
Esomeprazole126
Diphenhydramine citrate, ibuprofen119
Acetaminophen, ibuprofen123
Loratadine, pseudoephedrine sulfate115
Hydrogen peroxide1100
Acetaminophen, aspirin, caffeine148
Lidocaine hcl148
Salicylic acid 2%118
Cocoa butter, phenylephrine hcl121
Ibuprofen capsule11
Alcohol1293
Magnesium hydroxide141
Caffeine138
Lansoprazole158
Magnesium sulfate140
Fluticasone propionate171
Aspirin, citric acid, sodium bicarbonate119
Pseudoephedrine hcl129
Dextromethorphan hydrobromide, guaifenesin149
Carboxymethylcellulose sodium130
Esomeprazole magnesium177
Terbinafine hydrochloride139
Camphor, eucalyptus oil, menthol132
Famotidine, calcium carbonate and magnesium hydroxide120
Dextromethorphan polistirex127
Bacitracin, neomycin, polymyxin b, pramoxine hydrochloride13
Bacitracin zinc139
Clotrimazole 1%111
Salicylic acid1330
Polyethylene glycol 3350167
Guaifenesin, pseudoephedrine hydrochloride18
Acetaminophen, diphenhydramine hcl142
Brompheniramine maleate, dextromethorphan hydrobromide118
Loratadine and pseudoephedrine sulfate115
White petrolatum167
Mineral oil, petrolatum, phenylephrine hcl128
Benzocaine1110
Mineral oil134
Polyethylene glycol 400, propylene glycol125
Fexofenadine hydrochloride165
Glycerin, phenylephrine hcl, pramoxine hcl, white petrolatum113

Dosage forms

Dosage formProductsShare
Tablet, film coated1610.5%
Solution159.9%
Gum, chewing127.9%
Lozenge106.6%
Suspension95.9%
Capsule, liquid filled74.6%
Tablet, chewable74.6%
Tablet, film coated, extended release63.9%
Tablet63.9%
Gel63.9%
Mouthwash63.9%
Tablet, coated63.9%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Cetirizine HCl56062-495CapsuleNew drug applications (NDA)July 15, 2026
Nicotine56062-957LozengeGeneric drugs (ANDA)June 11, 2026
Nicotine56062-812Gum, chewingGeneric drugs (ANDA)June 11, 2026
Nicotine56062-734LozengeGeneric drugs (ANDA)June 11, 2026
Nicotine coated56062-681LozengeGeneric drugs (ANDA)June 11, 2026
Nicotine56062-671LozengeGeneric drugs (ANDA)June 11, 2026
Nicotine56062-646Gum, chewingGeneric drugs (ANDA)June 11, 2026
Nicotine56062-636LozengeGeneric drugs (ANDA)June 11, 2026
Nicotine coated56062-543LozengeGeneric drugs (ANDA)June 11, 2026
Nicotine56062-509LozengeGeneric drugs (ANDA)June 11, 2026
Nicotine56062-499LozengeGeneric drugs (ANDA)June 11, 2026
Coated nicotine56062-369Gum, chewingGeneric drugs (ANDA)June 11, 2026
Nicotine56062-298Gum, chewingGeneric drugs (ANDA)June 11, 2026
Nicotine56062-019Gum, chewingGeneric drugs (ANDA)June 11, 2026
Nasal and chest decongestant56062-614Tablet, multilayer, extended releaseGeneric drugs (ANDA)April 2, 2026
Cetylpyridinium Chloride56062-542LiquidOver the counter monograph drugsMarch 11, 2026
Acid reducer56062-088Tablet, film coatedGeneric drugs (ANDA)March 6, 2026
Arthritis pain reliever56062-471GelGeneric drugs (ANDA)September 12, 2025
Coated nicotine56062-110Gum, chewingGeneric drugs (ANDA)September 5, 2025
Childrens cold cough dm56062-502SolutionOver the counter monograph drugsJuly 28, 2025
Dual action56062-530Tablet, film coatedGeneric drugs (ANDA)May 16, 2025
Sleep aid56062-441TabletGeneric drugs (ANDA)May 16, 2025
Allergy56062-923Tablet, film coatedOver the counter monograph drugsApril 28, 2025
Nitetime severe56062-763SolutionOver the counter monograph drugsFebruary 3, 2025
Nighttime Sleep Aid56062-091Tablet, coatedOver the counter monograph drugsNovember 25, 2024

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.