Quick answers
- What is SoluPrep S?
- SoluPrep S is a brand name of Chlorhexidine and isopropyl alcohol, an over-the-counter medicine. The FDA NDC Directory lists 2 SoluPrep S products in 1 strength and form.
- Who makes SoluPrep S?
- Solventum holds the FDA application for SoluPrep S (NDA208288, approved August 8, 2018).
- Is there a generic or store brand of SoluPrep S?
- Yes. The FDA NDC Directory lists 3 other products with the same active ingredients, strength and form as a SoluPrep S product. Ask your pharmacist whether one is right for you.
- Has SoluPrep S been recalled?
- No recall linked to SoluPrep S products (by their NDC code or label) appears in the FDA enforcement reports we use.
What SoluPrep S is
Each SoluPrep S product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Chlorhexidine and isopropyl alcohol · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| chlorhexidine gluconate 20 mg/mL · isopropyl alcohol 70% solution (topical) | 3M SoluPrep S | 3 products, 2 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Chlorhexidine and isopropyl alcohol →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA208288 | Solventum | August 8, 2018 | 2 |
Companies that list SoluPrep S
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of SoluPrep S products.
- Solventum US LLC2 products
Recalls
No recall linked to SoluPrep S products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.