Chicory Ginger Bitters

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: Chicory Ginger Bitters
Generic name: CHICORY GINGER BITTERS
Manufacturer: Uriel Pharmacy, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: cfbb1c5a-6a34-bf50-e053-2a95a90a126b
SPL ID: 4409f89b-6404-add5-e063-6394a90ab70e
Version: 3
Effective date: 2025-11-20
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 06:18:09

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Chicory Ginger Bitters	openfda.brand_name
generic name		CHICORY GINGER BITTERS	openfda.generic_name
manufacturer name		Uriel Pharmacy, Inc.	openfda.manufacturer_name
ndc	package	48951-3251-9	openfda.package_ndc
ndc	package	48951-3251-3	openfda.package_ndc
ndc	product	48951-3251	openfda.product_ndc
ndc11	package	48951325103	derived:openfda.package_ndc
ndc11	package	48951325109	derived:openfda.package_ndc
spl id		4409f89b-6404-add5-e063-6394a90ab70e	id
spl set id		cfbb1c5a-6a34-bf50-e053-2a95a90a126b	set_id
unii		7E889U5RNN	openfda.unii
unii		S72O3284MS	openfda.unii
unii		F84709P2XV	openfda.unii
unii		KM66971LVF	openfda.unii
unii		856YO1Z64F	openfda.unii
unii		U946SH95EE	openfda.unii
unii		XY1K7KIQ0F	openfda.unii
unii		C5529G5JPQ	openfda.unii
unii		1KE45XD28S	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: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing. SHAKE WELL BEFORE USE. REFRIGERATE AFTER OPENING. BEST WHEN USED WITHIN 30 DAYS OF OPENING.

Reported adverse events (FAERS/openFDA)#

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