Aurum 5X Lavender 0.3 Rose 0.3

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: Aurum 5X Lavender 0.3 Rose 0.3
Generic name: AURUM 5X LAVENDER 0.3 ROSE 0.3
Manufacturer: Uriel Pharmacy, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 2ead84a6-ed7c-d51d-e063-6394a90a1b09
SPL ID: 2ead84a6-ed7d-d51d-e063-6394a90a1b09
Version: 1
Effective date: 2025-02-21
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:04:38

Harmonized routes table
Harmonized routes
TOPICAL

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Aurum 5X Lavender 0.3 Rose 0.3	openfda.brand_name
generic name		AURUM 5X LAVENDER 0.3 ROSE 0.3	openfda.generic_name
manufacturer name		Uriel Pharmacy, Inc	openfda.manufacturer_name
ndc	package	48951-1398-2	openfda.package_ndc
ndc	product	48951-1398	openfda.product_ndc
ndc11	package	48951139802	derived:openfda.package_ndc
spl id		2ead84a6-ed7d-d51d-e063-6394a90a1b09	id
spl set id		2ead84a6-ed7c-d51d-e063-6394a90a1b09	set_id
unii		79Y1949PYO	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. Contains traces of lactose Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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