Childhood Immunization Detox
Childhood Immunization Detox is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Childhood Immunization Detox 6032. Available dosage form: liquid.
Drug Details
- Generic Name
- Childhood Immunization Detox
- Brand Names
- Childhood Immunization Detox 6032
- Application Number
- Sponsor
- Professional Complementary Health Formulas
- NDC Codes
- 1
- Dosage Forms
- LIQUID
- Routes
- ORAL
- Active Ingredients
- OYSTER SHELL CALCIUM CARBONATE, CRUDE, ECHINACEA ANGUSTIFOLIA WHOLE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAF, ARSENIC TRIOXIDE, SULFUR, MELANDRIN, L-3972-T, HEPATITIS A VIRUS STRAIN HM175 ANTIGEN (FORMALDEHYDE INACTIVATED), MYCOBACTERIUM BOVIS BCG, MUMPS VIRUS, CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED), HUMAN VARICELLA-ZOSTER IMMUNE GLOBULIN
Indications and Usage
INDICATIONS For the temporary relief of fussiness, tiredness, loss of appetite, minor aches or pains, occasional headache, nausea, or vomiting due to sensitivity to vaccination.*
Warnings
WARNINGS Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, rash, or persistent headache, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.