Drugplain

Navy Bean .05 g/mL

Phaseolus vulgaris · SOLUTION · Greer Laboratories, Inc.

No Recall History
Plain English

Navy Bean (Phaseolus vulgaris) is an over-the-counter solution administered by injection into the skin. This product contains navy bean extract at a concentration of 0.05 g/mL.

Key Facts

Brand Name
Navy Bean
Generic Name
Phaseolus vulgaris
NDC Code (Product)
22840-5705
Manufacturer
Greer Laboratories, Inc.
Strength
.05 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

USES: For temporary relief of gastrointestinal dyspepsia with flatulence and bloating, loss of weight and intolerance of certain foods.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: • 10 drops orally, 3 times a day or as directed by a health care professional. • Consult a health care professional for use in children under 12 years of age.

Warnings

WARNINGS: If pregnant or breast-feeding, ask a health care 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 Navy Bean used for?

Navy Bean (Phaseolus vulgaris) is an over-the-counter solution administered by injection into the skin. This product contains navy bean extract at a concentration of 0.05 g/mL.

Is Navy Bean a controlled substance?

Navy Bean is not classified as a controlled substance by the DEA.

What is the generic name for Navy Bean?

The generic name for Navy Bean is Phaseolus vulgaris. There are 3 other brand versions of Phaseolus vulgaris.

What is the NDC code for Navy Bean .05 g/mL?

The NDC (National Drug Code) for Navy Bean .05 g/mL is 22840-5705, listed by Greer Laboratories, Inc..

Product NDC

22840-5705

Package NDC

22840-5705-2

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

Data from openFDA · Public domain (CC0 1.0)