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California Black Oak Pollen

NDC 22840-5449 · Greer Laboratories, Inc.

Generic nameQuercus kelloggii
Dosage formSOLUTION
RouteINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active ingredient(s)QUERCUS KELLOGGII POLLEN
Strength.05 g/mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS]
Marketing categoryBLA

Packages

22840-5449-2 — 10 mL in 1 VIAL, MULTI-DOSE (22840-5449-2)

22840-5449-4 — 50 mL in 1 VIAL, MULTI-DOSE (22840-5449-4)

22840-5449-5 — 5 mL in 1 BOTTLE, DROPPER (22840-5449-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

22840-2485 — Quercus kelloggii, 22840-4464 — Quercus kelloggii, 22840-9469 — Quercus kelloggii, Quercus agrifolia and Quercus garryana, 22840-9470 — Quercus kelloggii, Quercus agrifolia and Quercus garryana, 22840-9472 — Quercus kelloggii, Quercus agrifolia and Quercus garryana, 22840-9805 — Quercus kelloggii, Quercus agrifolia and Quercus garryana, 22840-9806 — Quercus kelloggii, Quercus agrifolia and Quercus garryana, 49643-264 — Quercus agrifolia/Quercus kelloggii, 63083-1020 — Southwest Regional, 63083-1021 — Northeast Regional, 63083-1024 — Southeast Regional, 63083-1026 — Eastern Trees

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.