Drugplain

Giant Ragweed .1 g/mL

Ambrosia trifida · SOLUTION · Greer Laboratories, Inc.

No Recall History
Plain English

Giant Ragweed is a solution containing ambrosia trifida at .1 g/mL, taken intradermal. Manufactured by Greer Laboratories, Inc..

Key Facts

Brand Name
Giant Ragweed
Generic Name
Ambrosia trifida
NDC Code (Product)
22840-1382
Manufacturer
Greer Laboratories, Inc.
Strength
.1 g/mL
Dosage Form
SOLUTION
Route
INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Marketing Status
Application #
BLA101833
Marketing Start
09/15/1981

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS: May temporarily relieve sinus congestion, runny nose, and sneezing.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Frequently Asked Questions

What is Giant Ragweed used for?

Giant Ragweed contains Ambrosia trifida. It is a solution taken intradermal. Consult your doctor for specific uses.

Is Giant Ragweed a controlled substance?

Giant Ragweed is not classified as a controlled substance by the DEA.

What is the generic name for Giant Ragweed?

The generic name for Giant Ragweed is Ambrosia trifida. There are 1 other brand versions of Ambrosia trifida.

What is the NDC code for Giant Ragweed .1 g/mL?

The NDC (National Drug Code) for Giant Ragweed .1 g/mL is 22840-1382, listed by Greer Laboratories, Inc..

Product NDC

22840-1382

Package NDC

22840-1382-2

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)