Home FDA labels f2450c84-42d4-4f78-9884-86febc04bef2 Reflux Away 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 Reflux Away
Generic name ABIES NIGRA, ANTIMONIUM CRUDUM, ARGENTUM NITRICUM, CARBO VEGETABILIS, CHELIDONIUM MAJUS, COLOCYNTHIS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA
Manufacturer NaturalCare
Product type HUMAN OTC DRUG
SPL set ID 8a00a72f-60df-4477-b7b8-abb6355e34da
SPL ID f2450c84-42d4-4f78-9884-86febc04bef2
Version 1
Effective date 2026-03-24
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 06:18:14 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 · 17 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Reflux Away openfda.brand_name generic name ABIES NIGRA, ANTIMONIUM CRUDUM, ARGENTUM NITRICUM, CARBO VEGETABILIS, CHELIDONIUM MAJUS, COLOCYNTHIS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA openfda.generic_name manufacturer name NaturalCare openfda.manufacturer_name ndc package 70163-0041-1 openfda.package_ndc ndc product 70163-0041 openfda.product_ndc ndc11 package 70163004101 derived:openfda.package_ndc spl id f2450c84-42d4-4f78-9884-86febc04bef2 id spl set id 8a00a72f-60df-4477-b7b8-abb6355e34da set_id unii 2P3VWU3H10 openfda.unii unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii F79059A38U openfda.unii unii 71AOV0W131 openfda.unii unii 95IT3W8JZE openfda.unii unii 451W47IQ8X 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: Stop use and ask a doctor if ■ symptoms worsen or persist for more than 5 days ■ new symptoms appear ■ blood is present in stool If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if printed foil blister is broken or missing. ■ Store at room temperature (65-80ºF)
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.