Vax Reaction
- Product NDC
- 43742-1337
- 11-digit product format
- 437421337
- Labeler code
- 43742
- Product ID
- 43742-1337_36302411-ef71-429d-8605-6be4bae2e5dd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Thuja Occidentalis, Mezereum, Silicea, Calcarea Carbonica, Morbillinum, Parotidinum, Pertussinum, Poliomyelitis Nosode, Rubella Nosode, Tetanus Toxin, Carcinosin, Antimonium Crudum, Ledum Palustre, Thimerosal
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-10-23
- Marketing end
- 2024-08-21
- Substance
- THUJA OCCIDENTALIS LEAFY TWIG; DAPHNE MEZEREUM BARK; SILICON DIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; MEASLES VIRUS; MUMPS VIRUS; BORDETELLA PERTUSSIS; POLIOVIRUS; RUBELLA VIRUS; CLOSTRIDIUM TETANI; HUMAN BREAST TUMOR CELL; ANTIMONY TRISULFIDE; LEDUM PALUSTRE TWIG; THIMEROSAL
- Active strength
- 6 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1337-1 | 43742133701 | 30 mL in 1 BOTTLE, DROPPER (43742-1337-1) | 30 ml | 2018-10-23 | 2024-08-21 | No | No | Current |