Dyna-Hex 2

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)

Brand name
Dyna-Hex 2
Generic name
CHLORHEXIDINE GLUCONATE 2%
Manufacturer
Xttrium Laboratories, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
0c808ebd-1bf7-175d-e063-6294a90ae7df
SPL ID
3400ba9f-d027-b3f7-e063-6394a90ac53a
Version
2
Effective date
2025-04-30
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:16:18
Harmonized routes table
Harmonized routes
TOPICAL

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

For external use only Allergy alert: This product may cause a severe allergic reaction. Symptoms may include:  wheezing/difficulty breathing  shock  facial swelling  hives  rash If an allergic reaction occurs, stop use and seek medical help right away. Do not use if you or the patient are allergic to chlorhexidine gluconate or any other ingredient in this product When using this product  keep out of eyes, ears, and mouth. May cause serious and permanent eye injury if permitted to enter and remain in the eye or may cause deafness when instilled in the middle ear through perforated eardrums.  if solution should contact these areas, rinse out promptly and thoroughly with water  wounds which involve more than the superficial layers of the skin should not be routinely treated Stop use and ask a doctor if irritation, sensitization, or allergic reaction occurs. These may be signs of a serious condition. Keep out of 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.