GUNA DIGESTION PLUS

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
GUNA DIGESTION PLUS
Generic name
PORK LIVER - LYCOPODIUM CLAVATUM SPORE - STRYCHNOS NUX VOMICA SEED - SUS SCROFA PANCREAS - AETHUSA CYNAPIUM -
Manufacturer
Guna spa
Product type
HUMAN OTC DRUG
SPL set ID
b8db0bfe-4e96-25dc-e053-2a95a90aa847
SPL ID
b8db0bfe-4e97-25dc-e053-2a95a90aa847
Version
1
Effective date
2021-02-17
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 06:18:04
Harmonized routes table
Harmonized routes
ORAL

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 Stop use and ask doctor if symptoms persist more than 5 days. If pregnant or breast-feeding ask a health care professional before use. Do not use more than the recommended dose. Keep out of reach of children. In case of overdose, seek professional assistance or contact a Poison Control Center right away. Contains ethyl alcohol 30%

Reported adverse events (FAERS/openFDA)#

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