FDA label d7142db6-14d7-43ab-b0dd-64459a2be200

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
e3807a1b-c375-456a-bd7e-de3a1607c8fc
SPL ID
d7142db6-14d7-43ab-b0dd-64459a2be200
Version
1
Effective date
2010-07-16
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:07:42

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Allergy alert - certain persons san develop allergic reactions to ingredients in this product Do not use - in or near the eyes - do not get into the eyes - in infants under 2 years of age - in large quantities, particularly over raw surfaces or blistered areas - do not put this product into rectum by using fingers or any mechanical device Stop use and ask a doctor if - condition worsens, or does not improve within 7 days - the symptom being treated does not subside or if redness, irritation, swelling, bleeding or other symptoms develop or increase If pregnant or breast feeding, as a health care professional before use Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.