Constipation 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: Constipation Relief
Generic name: ALOE, POTASSIUM ALUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVATED CHARCOAL, DIOSCOREA VILLOSA TUBER, VERONICASTRUM VIRGINICUM ROOT, STRYCHNOS NUX VOMICA SEED
Manufacturer: TRP Company
Product type: HUMAN OTC DRUG
SPL set ID: 12dea1d1-9510-5aad-e054-00144ff8d46c
SPL ID: 46051d5f-d0ec-e853-e063-6294a90a4922
Version: 5
Effective date: 2025-12-15
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:01

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		Constipation Relief	openfda.brand_name
generic name		ALOE, POTASSIUM ALUM, OYSTER SHELL CALCIUM CARBONATE, CRUDE ACTIVATED CHARCOAL, DIOSCOREA VILLOSA TUBER, VERONICASTRUM VIRGINICUM ROOT, STRYCHNOS NUX VOMICA SEED	openfda.generic_name
manufacturer name		TRP Company	openfda.manufacturer_name
ndc	package	17312-031-14	openfda.package_ndc
ndc	product	17312-031	openfda.product_ndc
ndc11	package	17312003114	derived:openfda.package_ndc
spl id		46051d5f-d0ec-e853-e063-6294a90a4922	id
spl set id		12dea1d1-9510-5aad-e054-00144ff8d46c	set_id
unii		2P3VWU3H10	openfda.unii
unii		IWY3IWX2G8	openfda.unii
unii		269XH13919	openfda.unii
unii		1L24V9R23S	openfda.unii
unii		2E32821G6I	openfda.unii
unii		M2O62YTN42	openfda.unii
unii		V5VD430YW9	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.

Reported adverse events (FAERS/openFDA)#

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