Beautox

FDA Drug Profile — Beautox 6007

Beautox is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Beautox 6007. Available dosage form: liquid.

Drug Details

Generic Name
Beautox
Brand Names
Beautox 6007
Application Number
Sponsor
Professional Complementary Health Formulas
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
ECHINACEA ANGUSTIFOLIA WHOLE, BOS TAURUS BRAIN, CAMPHOR (NATURAL), BEEF KIDNEY, BEEF LIVER, BEEF LUNG, BOS TAURUS PITUITARY GLAND, POSTERIOR, NITRIC ACID, PHOSPHORIC ACID, ACETYLDIGITOXIN

Indications and Usage

INDICATIONS For the temporary relief of cough, shortness of breath, irritation of the eyes, nose, or throat, itchy, dry, or irritated skin, dizziness, or occasional headache due to sensitivity to or exposure to chemicals used in cosmetology.*

Warnings

WARNINGS In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.