Astragalus Arnica

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2026-02-27
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 02:37:47

Label at a glance#

ProductAstragalus Arnica

Active ingredientASTRAGALUS PROPINQUUS ROOT, ARNICA MONTANA

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops.
Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Astragalus (Milk vetch) 3X, Arnica 30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, 20% Biodynamic organic grape alcohol

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858

Made with care by Uriel, East Troy, WI 53120

shopuriel.com

Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Astragalus Arnica Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1171-3	Astragalus Arnica	60 mL in 1 BOTTLE, GLASS	LIQUID	60		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ARNICA MONTANA	ACTIVE INGREDIENT	O80TY208ZW	1
ASTRAGALUS PROPINQUUS ROOT	ACTIVE INGREDIENT	922OP8YUPF	1
ARNICA MONTANA	ACTIVE MOIETY	O80TY208ZW	1
ASTRAGALUS PROPINQUUS ROOT	ACTIVE MOIETY	922OP8YUPF	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Astragalus Arnica
WATER
ALCOHOL
ASTRAGALUS PROPINQUUS ROOT
ARNICA MONTANA

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-1171	48951-1171-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
ASTRAGALUS PROPINQUUS ROOT	922OP8YUPF	ACTIB
ARNICA MONTANA	O80TY208ZW	ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Astragalus Arnica	ASTRAGALUS ARNICA	Uriel Pharmacy Inc.	f6296548-4d16-4690-a1a5-76d8bd718afa	2026-02-27	Warnings	Exact identifier ndc (package): 48951-1171-3 ndc (product): 48951-1171 ndc11 (package): 48951117103 spl id: 4bd3fa49-f046-6e91-e063-6294a90abe66 spl set id: f6296548-4d16-4690-a1a5-76d8bd718afa

Reported adverse events (FAERS/openFDA)#

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