NDC product
Baby Nighttime Oral Pain Relief
NDC 54973-3324 · Hyland' Inc.
Key facts
| Product NDC | 54973-3324 |
|---|---|
| Proprietary name | Baby Nighttime Oral Pain Relief |
| Nonproprietary name | Arnica Montana, Tribasic Calcium Phosphate, Matricaria Chamomilla, Silicon Dioxide, Magnesium Phosphate, Dibasic Trihydrate, Ferrosoferric Phosphate, Arabica Coffee Bean and Oyster Shell Calcium Carbonate, Crude |
| Substances | OYSTER SHELL CALCIUM CARBONATE, CRUDE, TRIBASIC CALCIUM PHOSPHATE, MATRICARIA CHAMOMILLA, SILICON DIOXIDE, ARNICA MONTANA, FERROSOFERRIC PHOSPHATE, ARABICA COFFEE BEAN, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Hyland' Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE] and 10 more |
| Marketing start | Aug 17, 2017 |
| 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: