NDC product
Travel Immunization Detox 6033
NDC 63083-6033 · Professional Complementary Health Formulas
Key facts
| Product NDC | 63083-6033 |
|---|---|
| Proprietary name | Travel Immunization Detox |
| Nonproprietary name | Travel Immunization Detox |
| Substances | OYSTER SHELL CALCIUM CARBONATE, CRUDE, ECHINACEA ANGUSTIFOLIA WHOLE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAF, ARSENIC TRIOXIDE, SULFUR, MELANDRIN, CHOLERA ENTEROTOXIN SUBUNIT B, HEPATITIS A VIRUS STRAIN HM175 ANTIGEN (FORMALDEHYDE INACTIVATED), JAPANESE ENCEPHALITIS VIRUS STRAIN NAKAYAMA-NIH ANTIGEN (FORMALDEHYDE INACTIVATED), ANOPHELES QUADRIMACULATUS, MUMPS VIRUS and 4 more |
| 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], Allergens [CS], Cell-mediated Immunity [PE], Hepatitis A Vaccines [CS], Inactivated Clostridium Tetani Vaccine [EPC], Inactivated Hepatitis A Virus Vaccine [EPC] and 14 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: