HydrAphex

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
HydrAphex
Generic name
HYDRAPHEX
Manufacturer
Aphex Biocleanse Systems, Inc
Product type
HUMAN OTC DRUG
SPL set ID
a6035c7d-0f5b-3295-e053-2995a90af89c
SPL ID
d5ccc62d-3d96-650c-e053-2a95a90a5e17
Version
2
Effective date
2022-01-17
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:30:21
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

Warnings Warnings: For External Use Only Do not use in eyes. In case of eye contact, immediately flush with water and seek medical advice. Discontinue use if skin irritation or redness develops. Not for use on sensitive areas of the body or burns. If swallowed, get medical help or contact a poison control center right away. Keep Out of Reach of Children

Reported adverse events (FAERS/openFDA)#

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