NDC product
Abdominal Pain Drops 2051
NDC 63083-2051 · Professional Complementary Health Formulas
Key facts
| Product NDC | 63083-2051 |
|---|---|
| Proprietary name | Abdominal Pain Drops |
| Nonproprietary name | Abdominal Pain Drops |
| Substances | ARTEMISIA ANNUA FLOWERING TOP, LYCOPODIUM CLAVATUM SPORE, ACTIVATED CHARCOAL, SODIUM SULFATE, BOS TAURUS SOLAR PLEXUS, TRIPE, SUS SCROFA PARASYMPATHETIC NERVE, HYDROCHLORIC ACID, STRYCHNOS NUX-VOMICA SEED |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Professional Complementary Health Formulas |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] and 1 more |
| Marketing start | Aug 15, 1984 |
| 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: