FDA label 2ee5b6bd-e2dd-294b-e063-6294a90a190f
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- SPL set ID
- 00baca82-57bd-4af1-95cb-eaa0ba8a3a19
- SPL ID
- 2ee5b6bd-e2dd-294b-e063-6294a90a190f
- Version
- 2
- Effective date
- 2025-02-24
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:20:42
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| spl id | 2ee5b6bd-e2dd-294b-e063-6294a90a190f | id | |
| spl set id | 00baca82-57bd-4af1-95cb-eaa0ba8a3a19 | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings For external use only Ask a doctor before use if you have seborrheic dermatitis in areas other than the scalp When using this product •do not get into eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if •condition worsens or does not improve after regular use as directed Keep out of reach of children. If swallowed, bet medical help or contact a Poison Control Center right away.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTION PACKAGED FOR DOLGENCORP, LLC 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072 USA visit us at Rexall.com or call 1-866-4-REXALL
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.