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Plantain Sorrel Mix

NDC 22840-9352 · Greer Laboratories, Inc.

Generic namePlantago lanceolata and Rumex acetosella
Dosage formSOLUTION
RouteINTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS
Active ingredient(s)RUMEX ACETOSELLA POLLEN, PLANTAGO LANCEOLATA POLLEN
Strength.025; .025 g/mL; g/mL
Pharmacologic classAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS], Pollen [CS]
Marketing categoryBLA

Packages

22840-9352-2 — 10 mL in 1 VIAL, MULTI-DOSE (22840-9352-2)

22840-9352-4 — 50 mL in 1 VIAL, MULTI-DOSE (22840-9352-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

22840-9313 — Xanthium strumarium, Plantago lanceolata, Chenopodium album, Amaranthus retroflexus and Salsola kali, 22840-9314 — Xanthium strumarium, Plantago lanceolata, Chenopodium album, Amaranthus retroflexus and Salsola kali, 22840-9315 — Rumex acetosella and Rumex crispus, 22840-9316 — Rumex acetosella and Rumex crispus, 22840-9317 — Rumex acetosella and Rumex crispus, 22840-9319 — Rumex acetosella and Rumex crispus, 22840-9325 — Plantago lanceolata and Rumex acetosella, 22840-9326 — Plantago lanceolata and Rumex acetosella, 22840-9327 — Plantago lanceolata and Rumex acetosella, 22840-9328 — Plantago lanceolata and Rumex acetosella, 22840-9353 — Plantago lanceolata and Rumex acetosella, 49643-389 — Plantago lanceolata, 49643-405 — Rumex acetosella, 65044-1516 — Pollens - Weeds, Dock/Sorrel Mix, 65044-1517 — Pollens - Weeds, Dock/Sorrel Mix, 65044-1519 — Pollens - Weeds, Dock/Sorrel Mix, 65044-1520 — Pollens - Weeds, Dock/Sorrel Mix, 65044-2212 — Plantain, English Plantago lanceolata, 65044-2213 — Plantain, English Plantago lanceolata, 65044-2215 — Plantain, English Plantago lanceolata, +36 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels