Travel Immunization Detox

FDA Drug Profile — Travel Immunization Detox 6033

Travel Immunization Detox is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Travel Immunization Detox 6033. Available dosage form: liquid.

Drug Details

Generic Name
Travel Immunization Detox
Brand Names
Travel Immunization Detox 6033
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, 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, POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED), CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED), SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI, YELLOW FEVER VIRUS STRAIN 17D-204 LIVE ANTIGEN

Indications and Usage

INDICATIONS For the temporary relief of aches, pains, or stiffness of muscles or joints, occasional headache, tiredness, chills, mild itching, 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.