FDA label 0ec59b2a-dbbc-841f-e063-6294a90ab12a
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
- 8da693d4-e4b1-fa06-e053-2a95a90a00fa
- SPL ID
- 0ec59b2a-dbbc-841f-e063-6294a90ab12a
- Version
- 9
- Effective date
- 2024-01-12
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:23:38
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 | 0ec59b2a-dbbc-841f-e063-6294a90ab12a | id | |
| spl set id | 8da693d4-e4b1-fa06-e053-2a95a90a00fa | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Triple Warnings For external use only Allergy aler t: do not use if you are allergic to any of the ingredients Do not use in the eyes over large areas of the body Ask a doctor before use if you have a deep or puncture wounds animal bites serious burns Stop use and ask a doctor if the condition persists or gets worse a rash or other allergic reaction develops you need to use longer than 1 week Keep out of the reach of children If swallowed, get medical help or contact a Poison Control Center right away.
warnings
BZK Wipe Warnings For external use only Do not use in the eyes or over large areas of the body on mucous membranes on irritated skin in case of deep puncture wounds, animal bites or serious burns, consult a doctor longer than 1 week unless directed by a doctor Stop use and ask a doctor if if irritation, redness or other symptoms develop the condition persists or gets worse Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
warnings
Eyewash Warnings For external use only Obtain immediate medical treatment for all open wounds in or near eyes. To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard. Do not use if solution changes color or becomes cloudy if you have open wounds in or near the eyes, get medical help right away. Stop use and ask a doctor if you experience eye pain changes in vision continued redness or irritation of the eye condition worsens or persists Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
warnings
Hydrocortisone Warnings For external use only Ask a doctor before use if you are using any other hydrocortisone product When using the product avoid contact with eyes do not begin use of any other hydrocortisone product unless you have consulted a doctor do not use for the treatment of diaper rash Stop use and ask a doctor if condition worsens condition persists for more than 7 days condition clears up and recurs within a few days Keep out of reach of children If swallowed, get 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 Reactions Possible adverse effects arising from the irrigation of body cavities, tissues, or indwelling catheters and tubes can be minimized when proper procedures are followed. Displaced catheters or drainage tubes can lead to irrigation or infiltration of unintended structures or cavities. Excessive volume or pressure during irrigation of closed cavities may cause undue distension or disruption of tissues. Accidental contamination from careless technique may transmit infection. If an adverse reaction does occur, discontinue administration of the irrigant, evaluate the patient, institute appropriate therapeutic countermeasures, and save the remainder of the fluid for examination if deemed necessary.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.