Birch Juniper

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: Birch Juniper
Generic name: BIRCH JUNIPER
Manufacturer: Uriel Pharmacy Inc
Product type: HUMAN OTC DRUG
SPL set ID: 0fa00042-b326-6d2d-e063-6394a90a236d
SPL ID: 43e13f9e-f46f-c5ad-e063-6394a90a25d7
Version: 5
Effective date: 2025-11-18
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:56:17

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Birch Juniper	openfda.brand_name
generic name		BIRCH JUNIPER	openfda.generic_name
manufacturer name		Uriel Pharmacy Inc	openfda.manufacturer_name
ndc	package	48951-2149-9	openfda.package_ndc
ndc	product	48951-2149	openfda.product_ndc
ndc11	package	48951214909	derived:openfda.package_ndc
spl id		43e13f9e-f46f-c5ad-e063-6394a90a25d7	id
spl set id		0fa00042-b326-6d2d-e063-6394a90a236d	set_id
unii		40S83Y133C	openfda.unii
unii		O84B5194RL	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.