TRIP EASE

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: TRIP EASE
Generic name: SODIUM BORATE, ANAMIRTA COCCULUS SEED, GELSEMIUM SEMPERVIRENS ROOT, WOOD CREOSOTE, TOXICODENDRON PUBESCENS LEAF, AND TOBACCO LEAF
Manufacturer: Miers Laboratories
Product type: HUMAN OTC DRUG
SPL set ID: f49b0bd9-00fd-4703-a1ca-f5f14e7ebb5d
SPL ID: faf5e575-9860-4fb2-810a-29e02ba7cb21
Version: 2
Effective date: 2023-09-20
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:26

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		TRIP EASE	openfda.brand_name
generic name		SODIUM BORATE, ANAMIRTA COCCULUS SEED, GELSEMIUM SEMPERVIRENS ROOT, WOOD CREOSOTE, TOXICODENDRON PUBESCENS LEAF, AND TOBACCO LEAF	openfda.generic_name
manufacturer name		Miers Laboratories	openfda.manufacturer_name
ndc	package	59672-1716-2	openfda.package_ndc
ndc	product	59672-1716	openfda.product_ndc
ndc11	package	59672171602	derived:openfda.package_ndc
spl id		faf5e575-9860-4fb2-810a-29e02ba7cb21	id
spl set id		f49b0bd9-00fd-4703-a1ca-f5f14e7ebb5d	set_id
unii		91MBZ8H3QO	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		6YR2608RSU	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		810258W28U	openfda.unii
unii		3JYG22FD73	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 Do not use if the blister pack is broken. Ask a doctor before use in children under 2 years of age Stop use and ask a doctor if symptoms persist for more than 3 days or worsen. If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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