Humphreys Maravilla

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
Humphreys Maravilla
Generic name
WITCH HAZEL
Manufacturer
Humphreys Pharmacal, Incorporated
Product type
HUMAN OTC DRUG
SPL set ID
7d403bf4-8a0d-4337-8e81-1149cd0ae1dc
SPL ID
ceb593f8-3283-4375-a27e-50597a6468d8
Version
9
Effective date
2024-12-06
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:31:04
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

Advertencias / Warnings: Para uso externo solamente / For external use only. Cuando use este producto evite el contacto con los ojos / When using this product avoid contact with eyes.

Reported adverse events (FAERS/openFDA)#

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