Vax Reaction
- Product NDC
- 43742-0159
- 11-digit product format
- 437420159
- Labeler code
- 43742
- Product ID
- 43742-0159_46c0d273-e7e6-419e-8493-169ce851346b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Mezereum, Thuja Occidentalis, Silicea, Calcarea Carbonica, Morbillinum, Parotidinum, Pertussinum, Poliomyelitis Nosode, Rubella Nosode, Tetanus Nosode, Carcinosin, Antimonium Crudum, Ledum Palustre, Thimerosal
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-09-20
- Marketing end
- 2020-07-23
- Substance
- DAPHNE MEZEREUM BARK; THUJA OCCIDENTALIS LEAF; SILICON DIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; MEASLES VIRUS; MUMPS VIRUS; POLIOVIRUS; RUBELLA VIRUS; CLOSTRIDIUM TETANI; HUMAN BREAST TUMOR CELL; ANTIMONY TRISULFIDE; LEDUM PALUSTRE TWIG; THIMEROSAL
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/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