Drugplain

Velvetgrass .001 g/mL

Holcus lanatus · SOLUTION · Greer Laboratories, Inc.

No Recall History
Plain English

Velvetgrass (Holcus Lanatus) is an over-the-counter solution administered by intradermal injection at a strength of 0.001 g/mL. This product is derived from velvet grass plant material, though its specific therapeutic uses and clinical efficacy have not been established in standard medical literature.

Key Facts

Brand Name
Velvetgrass
Generic Name
Holcus lanatus
NDC Code (Product)
22840-1231
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 History

Frequently Asked Questions

What is Velvetgrass used for?

Velvetgrass (Holcus Lanatus) is an over-the-counter solution administered by intradermal injection at a strength of 0.001 g/mL. This product is derived from velvet grass plant material, though its specific therapeutic uses and clinical efficacy have not been established in standard medical literature.

Is Velvetgrass a controlled substance?

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

What is the generic name for Velvetgrass?

The generic name for Velvetgrass is Holcus lanatus. There are 1 other brand versions of Holcus lanatus.

What is the NDC code for Velvetgrass .001 g/mL?

The NDC (National Drug Code) for Velvetgrass .001 g/mL is 22840-1231, listed by Greer Laboratories, Inc..

Product NDC

22840-1231

Package NDC

22840-1231-1

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

Data from openFDA · Public domain (CC0 1.0)