NDC product
Childhood Vaccination Nosode Combination 9409
NDC 63083-9409 · Professional Complementary Health Formulas
Key facts
| Product NDC | 63083-9409 |
|---|---|
| Proprietary name | Childhood Vaccination Nosode Combination |
| Nonproprietary name | Childhood Vaccination Nosode Combination |
| Substances | ANTIMONY POTASSIUM TARTRATE, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, QUININE SULFATE, SULFUR, CROTALUS HORRIDUS HORRIDUS VENOM, MERCURIUS SOLUBILIS, POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED), SILICON DIOXIDE, THUJA OCCIDENTALIS LEAF, VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Professional Complementary Health Formulas |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Actively Acquired Immunity [PE], Antimalarial [EPC], Inactivated Poliovirus Vaccine [EPC], Live Vaccinia Virus Vaccine [EPC], Poliovirus Vaccines [CS], Smallpox Vaccine [CS] and 4 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: