United States · FDA National Drug Code directory
OAK MIX
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0268-8070_91e6f082-b201-409a-9cab-95d4e0433468
- Product NDC
- 0268-8070
- Form
- INJECTION, SOLUTION
- Composition / generic term
- QUERCUS RUBRA, QUERCUS ALBA, QUERCUS VIRGINIANA
- Labeler
- ALK-Abello, Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 19980223
- Source listing expiry
- 20261231
Source-listed ingredients
- QUERCUS RUBRA POLLEN — .05 g/mL
- QUERCUS ALBA POLLEN — .05 g/mL
- QUERCUS VIRGINIANA POLLEN — .05 g/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10.5 mL in 1 VIAL (0268-8070-10) · 0268-8070-10
- 53 mL in 1 VIAL (0268-8070-50) · 0268-8070-50
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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