Natural Relief Diarrhea Relief

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: Natural Relief Diarrhea Relief
Generic name: ALOE, CITRULLUS COLOCYNTHIS, CROTON TIGLIUM, LYCOPODIUM CLAVATUM, MAGNESIUM SULFATE HEPTAHYDRATE, PHOSPHORIC ACID, THUJA OCCIDENTALIS
Manufacturer: TRP Company
Product type: HUMAN OTC DRUG
SPL set ID: 436de0c5-acd6-e32b-e063-6394a90aa275
SPL ID: 436de66a-ce49-e92c-e063-6394a90a2494
Version: 1
Effective date: 2025-11-12
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:29

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Natural Relief Diarrhea Relief	openfda.brand_name
generic name		ALOE, CITRULLUS COLOCYNTHIS, CROTON TIGLIUM, LYCOPODIUM CLAVATUM, MAGNESIUM SULFATE HEPTAHYDRATE, PHOSPHORIC ACID, THUJA OCCIDENTALIS	openfda.generic_name
manufacturer name		TRP Company	openfda.manufacturer_name
ndc	package	17312-473-14	openfda.package_ndc
ndc	product	17312-473	openfda.product_ndc
ndc11	package	17312047314	derived:openfda.package_ndc
spl id		436de66a-ce49-e92c-e063-6394a90a2494	id
spl set id		436de0c5-acd6-e32b-e063-6394a90aa275	set_id
unii		1NT28V9397	openfda.unii
unii		SK47B8698T	openfda.unii
unii		V5VD430YW9	openfda.unii
unii		0HK2GZK66E	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		C88X29Y479	openfda.unii
unii		23H32AOH17	openfda.unii

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 USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN AND UNDER THE SUPERVISION OF A PHYSICIAN. This product is intended to complement, not replace, standard medical treatment. Initial worsening of symptoms may occur. A physician should always be consulted to rule out serious causes. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if: You experience worsening symptoms. Symptoms last longer than 7 days. You get abdominal swelling or bulging.

Reported adverse events (FAERS/openFDA)#

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