NDC product
LIQUID · Procter & Gamble Manufacturing Company
NDC 37000-999 · Procter & Gamble Manufacturing Company
Key facts
| Product NDC | 37000-999 |
|---|---|
| Nonproprietary name | Eucalyptus Oil |
| Substances | EUCALYPTUS OIL |
| Dosage form | LIQUID |
| Labeler | Procter & Gamble Manufacturing Company |
| Product type | BULK INGREDIENT |
| Marketing category | BULK INGREDIENT |
| Marketing start | Oct 30, 2020 |
| Listing certified through | Dec 31, 2026 |
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: