NDC product
Rexall Ready to use 4pk LAXATIVE
NDC 55910-999 · Dolgencorp, LLC
Key facts
| Product NDC | 55910-999 |
|---|---|
| Proprietary name | Rexall Ready to use 4pk |
| Nonproprietary name | SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM and SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM |
| Substances | SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM |
| Dosage form | ENEMA |
| Route | RECTAL |
| Labeler | Dolgencorp, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M007 |
| Marketing start | Jun 25, 2018 |
| 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: