NDC product
Breath HP
NDC 44911-0591 · Energique, Inc.
Key facts
| Product NDC | 44911-0591 |
|---|---|
| Proprietary name | Breath HP |
| Nonproprietary name | Ammonium Muriaticum, Antimonium Tartaricum, Arsenicum Album, Bryonia (Alba), Calcarea Carbonica, Lobelia Inflata, Natrum Sulphuricum, Phosphorus, Spongia Tosta |
| Substances | AMMONIUM CHLORIDE, ANTIMONY POTASSIUM TARTRATE, ARSENIC TRIOXIDE, BRYONIA ALBA ROOT, OYSTER SHELL CALCIUM CARBONATE, CRUDE, LOBELIA INFLATA WHOLE, SODIUM SULFATE, PHOSPHORUS, SPONGIA OFFICINALIS SKELETON, ROASTED |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Jun 1, 2021 |
| 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: