White Oak Pollen

NDC 22840-3409 · Greer Laboratories, Inc.

Generic nameQuercus alba

Dosage formSOLUTION

RouteINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS

Active ingredient(s)QUERCUS ALBA POLLEN

Strength20000 [PNU]/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

22840-3409-2 — 10 mL in 1 VIAL, MULTI-DOSE (22840-3409-2)

22840-3409-4 — 50 mL in 1 VIAL, MULTI-DOSE (22840-3409-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0268-1327 — Oak White, 0268-1328 — Oak White, 0268-1329 — Oak White, 0268-6644 — White Oak, 0268-8070 — QUERCUS RUBRA, QUERCUS ALBA, QUERCUS VIRGINIANA, 22840-3408 — Quercus alba, 22840-3410 — Quercus alba, 22840-3411 — Quercus alba, 22840-3412 — Quercus alba, 22840-5482 — Quercus alba, 22840-9441 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9442 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9443 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9444 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9445 — Quercus velutina, Quercus rubra and Quercus alba, 22840-9447 — Quercus velutina, Quercus rubra and Quercus alba, 49643-402 — Quercus alba, 65044-2035 — Oak Mix, 65044-2036 — Oak Mix, 65044-2038 — Oak Mix, +1 more

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