ARNICA NETTLE BURN AND BITE- arnica nettle burn and bite spray
Uriel Pharmacy Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Arnica Nettle Burn and Bite

Directions: FOR TOPICAL USE ONLY.

Use up to every hour. Ages 2 and older: 1-2 sprays. Under age 2: Consult a doctor.

Active Ingredients: 100 gm contains: 4.5 gm Urtica urens (Small nettle) 1X, 1.5 gm Arnica 1X; Calendula 2X, Resina laricis (Larch resin) 2X, Thuja (American arborvitae) 2X, Symphytum (Comfrey) 2X, Cantharis (Spanish fly) 7X, Colloidal silver 8X

Inactive Ingredients: Distilled water, Organic cane alcohol

Uses: Temporary relief of minor burns and insect bites.

KEEP OUT OF REACH OF CHILDREN.

Warnings: FOR EXTERNAL USE ONLY. 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, 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 seals on box are broken or missing.
FOR BURNS, SEEK MEDICAL ATTENTION IF NEEDED.

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com

ArnicaNettleSpray

ARNICA NETTLE BURN AND BITE
arnica nettle burn and bite spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-1282
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9)	URTICA URENS	1 [hp_X] in 1 mL
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ)	ARNICA MONTANA FLOWER	1 [hp_X] in 1 mL
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ)	CALENDULA OFFICINALIS FLOWERING TOP	2 [hp_X] in 1 mL
LARIX DECIDUA RESIN (UNII: AD8LJ73GQF) (LARIX DECIDUA RESIN - UNII:AD8LJ73GQF)	LARIX DECIDUA RESIN	2 [hp_X] in 1 mL
THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (THUJA OCCIDENTALIS WHOLE - UNII:5HBV6WCE3N)	THUJA OCCIDENTALIS WHOLE	2 [hp_X] in 1 mL
COMFREY ROOT (UNII: M9VVZ08EKQ) (COMFREY ROOT - UNII:M9VVZ08EKQ)	COMFREY ROOT	2 [hp_X] in 1 mL
LYTTA VESICATORIA (UNII: 3Q034RO3BT) (LYTTA VESICATORIA - UNII:3Q034RO3BT)	LYTTA VESICATORIA	7 [hp_X] in 1 mL
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	8 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-1282-2	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/01/2009	03/12/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	03/12/2024

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-1282)

Revised: 3/2024

Document Id: 13909074-eeb2-c1ff-e063-6394a90ac7f0

Set id: e8d31bdf-4e7b-4524-8639-acc68195e28e

Version: 5

Effective Time: 20240313

Uriel Pharmacy Inc.