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Data / Drug companies / The Sisquoc Healthcare Corporation

The Sisquoc Healthcare Corporation: 5 products in the FDA NDC directory, labeler code 71229

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

The Sisquoc Healthcare Corporation (labeler code 71229) lists 5 products in the FDA National Drug Code Directory, covering 3 finished drugs by generic name. By type: 5 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on March 25, 2019.

The request: Watch The Sisquoc Healthcare Corporation (FDA labeler code 71229): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
71229
Products in commercial distribution
5
Packages
5
Finished drugs by generic name
3
Prescription products
0
Over the counter products
5
Flagged as original packager
5 of 5 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
March 25, 2019
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 drugs5100%

Products by type

TypeProductsShare
Over the counter drugs5100%

Drugs it lists

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

DrugProductsCompanies listing it
Tolnaftate399
Salicylic acid1330
Undecylenic acid138

Dosage forms

Dosage formProductsShare
Ointment240%
Cream240%
Solution120%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Warticide71229-105SolutionOver the counter monograph drugsMarch 25, 2019
Funginix jock itch treatment71229-104CreamOver the counter monograph drugsMarch 25, 2019
Funginix af71229-103CreamOver the counter monograph drugsMarch 25, 2019
Funginix anti-fungal treatment71229-102OintmentOver the counter monograph drugsMarch 25, 2019
Phytozine ringworm treatment maximum strength71229-101OintmentOver the counter monograph drugsMarch 25, 2019

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.