Sunflower .001 g/mL
Helianthus annuus · SOLUTION · Greer Laboratories, Inc.
No Recall History
Plain English
Sunflower is a solution containing helianthus annuus at .001 g/mL, taken intradermal. Manufactured by Greer Laboratories, Inc..
Key Facts
- Brand Name
- Sunflower
- Generic Name
- Helianthus annuus
- NDC Code (Product)
22840-1506- Manufacturer
- Greer Laboratories, Inc.
- Strength
- .001 g/mL
- Dosage Form
- SOLUTION
- Route
- INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
- Marketing Status
- Application #
- BLA101833
- Marketing Start
- 09/15/1981
Recall History
No Recall HistoryFrequently 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 .001 g/mL?
The NDC (National Drug Code) for Sunflower .001 g/mL is 22840-1506, listed by Greer Laboratories, Inc..
Other Helianthus Brands
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- Helianthus Annuus6 [hp_C]/137662-0800
- Helianthus Annuus30 [hp_C]/137662-0802
- Helianthus Annuus1 [hp_Q]/137662-0807
- Massage cream for stretch marks2000 mg/100mL84509-005
- Body Oil for Stretch Marks1200 mg/60mL84509-101
- Helianthus Annuus12 [hp_C]/137662-0801
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)