FDA label 0ec5c2eb-bde9-9ab8-e063-6294a90af0ca

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 (canonical bytes are SHA-256 checked before publication)

SPL set ID
96726c58-8d32-068f-e053-2a95a90ab622
SPL ID
0ec5c2eb-bde9-9ab8-e063-6294a90af0ca
Version
5
Effective date
2024-01-12
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 05:17:39

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 3 · 9 matching rows.

warnings

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

Warnings NaCl Irrigant FOR IRRIGATION ONLY. NOT FOR INJECTION. Irrigating fluids have been demonstrated to enter the systemic circulation in relatively large volumes; thus, irrigation solutions must be regarded as systemic drugs. Absorption of large amounts can cause fluid and/or solute overload resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentrations of the administered parenteral solutions. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentration. Do not warm above 150°F (66°C). After opening container, its contents should be used promptly to minimize the possibility of bacterial growth or pyrogen formation. Discard unused portion of irrigating solution since it contains no preservatives.

warnings

Alcohol Wipe Warnings For external use only Flammable , keep away from fire and flame Do not use in or near eyes over large areas of the body Ask a doctor before use if you have deep or puncture wounds animal bites serious burns When using this product do not use longer than 1 week unless directed by a doctor Stop use and consult a doctor if condition persists or gets worse Keep out of the reach of children If swallowed, get medical help or contact a Poison Control center right away

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 1 matching rows.

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.