Drugplain

Sunflower 1000 [PNU]/mL

Helianthus annuus · SOLUTION · Greer Laboratories, Inc.

No Recall History
Plain English

Sunflower is a solution containing helianthus annuus at 1000 [PNU]/mL, taken intradermal. Manufactured by Greer Laboratories, Inc..

Key Facts

Brand Name
Sunflower
Generic Name
Helianthus annuus
NDC Code (Product)
22840-1505
Manufacturer
Greer Laboratories, Inc.
Strength
1000 [PNU]/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

Stop use and ask a doctor if rash occurs

Dosage & Administration

Directions Apply liberally 15 minutes before sun exposure Reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m. Wear Long-sleeved shirts, pants, hats, and sunglasses Children under 6 months: Ask a doctor

Warnings

For External use only Do not use on damaged or broken skin When using this product, Keep out of eyes. Rinse with water to remove If swallowed, get medical help or contact a Poison Control Center right away

Frequently Asked Questions

What is Sunflower used for?

Sunflower contains Helianthus annuus. It is a solution taken intradermal. Consult your doctor for specific uses.

Is Sunflower a controlled substance?

Sunflower is not classified as a controlled substance by the DEA.

What is the generic name for Sunflower?

The generic name for Sunflower is Helianthus annuus. There are 8 other brand versions of Helianthus annuus.

What is the NDC code for Sunflower 1000 [PNU]/mL?

The NDC (National Drug Code) for Sunflower 1000 [PNU]/mL is 22840-1505, listed by Greer Laboratories, Inc..

Product NDC

22840-1505

Package NDC

22840-1505-1

Other Helianthus Brands

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

Data from openFDA · Public domain (CC0 1.0)