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Data / Drug companies / Swiss-American Cdmo, LLC

Swiss-American Cdmo, LLC: 15 products in the FDA NDC directory, labeler code 60232

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

Swiss-American Cdmo, LLC (labeler code 60232) lists 15 products in the FDA National Drug Code Directory, covering 12 finished drugs by generic name. By type: 15 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on December 11, 2025.

The request: Watch Swiss-American Cdmo, LLC (FDA labeler code 60232): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
60232
Products in commercial distribution
15
Packages
19
Finished drugs by generic name
12
Prescription products
0
Over the counter products
15
Flagged as original packager
15 of 15 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
May 7, 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 drugs15100%

Products by type

TypeProductsShare
Over the counter drugs15100%

Drugs it lists

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

DrugProductsCompanies listing it
Homosalate, octisalate, octocrylene, zinc oxide sunscreen21
Sunscreen229
Octinoxate, octisalate, zinc oxide sunscreen12
Octisalate, avobenzone, homosalate, octocrylene sunscreen11
Homosalate, octocrylene, avobenzone, octisalate sunscreen11
2% miconazole nitrate cream11
Salicylic acid acne gel11
Zinc oxide, titanium dioxide sunscreen13
Homosalate, zinc oxide sunscreen11
Titanium dioxide, titanium dioxide sunscreen11
Homosalate, octisalate, zinc oxide sunscreen11
Miconazole nitrate antifungal cream11

Dosage forms

Dosage formProductsShare
Cream746.7%
Lotion640%
Spray16.7%
Gel16.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Image Clear Cell Acne Spot Treatment60232-5022GelOver the counter monograph drugsDecember 11, 2025
Private Label Antifungal Barrier Cream60232-0046CreamOver the counter monograph drugsMay 9, 2025
Chemical Sunscreen SPF50 with Antipollution60232-4400LotionOver the counter monograph drugsOctober 18, 2024
Chemical Sunscreen SPF5060232-0043SprayOver the counter monograph drugsMarch 29, 2024
Physical Sunscreen SPF50 80 min WR 159-10060232-0044LotionOver the counter monograph drugsNovember 9, 2023
Private Label Sunscreen SPF35 40min WR RE126-20260232-0036LotionOver the counter monograph drugsNovember 9, 2023
Image MD Restoring Lip Enhancer SPF1560232-3537CreamOver the counter monograph drugsMarch 17, 2022
Private Label SPF 50 80 min Water Resistant60232-0035CreamOver the counter monograph drugsDecember 1, 2020
Image Prevention Refiner Primer SPF5060232-1830CreamOver the counter monograph drugsMarch 6, 2020
Image Prevention Plus Professional Ultimate Protection Moisturizer SPF5060232-1026CreamOver the counter monograph drugsJanuary 31, 2020
Image Skincare Prevention Plus Daily Ultimate Protection60232-1022CreamOver the counter monograph drugsJanuary 31, 2020
Private Label SPF45 Water Resistant Paraben Free Sunscreen60232-0006LotionOver the counter monograph drugsAugust 31, 2011
Private Label Super Light Oil-Free SPF4560232-0008LotionOver the counter monograph drugsMarch 22, 2011
Private Label Antifungal Barrier Cream60232-0009CreamOver the counter monograph drugsNovember 22, 2010
Private Label Moisturizing Oil Free Paraben Free SPF4360232-0007LotionOver the counter monograph drugsMay 7, 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.