NDC product
Suave Dry Antiperspirant Deodorant Powder and Petals
NDC 83711-142 · Suave Brands Co, LLC
Key facts
| Product NDC | 83711-142 |
|---|---|
| Proprietary name | Suave Dry Antiperspirant Deodorant Powder and Petals |
| Nonproprietary name | Dry Spray Antiperspirant Deodorant |
| Substances | ALUMINUM CHLOROHYDRATE |
| Dosage form | SPRAY |
| Route | TOPICAL |
| Labeler | Suave Brands Co, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M019 |
| Marketing start | Oct 21, 2025 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: