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
2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:33

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.