URTICA URENS 30C

Manufacturer
Boiron | Boiron, Inc.
Effective date
2026-04-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:38:19

Label at a glance#

ProductURTICA URENS
Active ingredientURTICA URENS
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient** (in each pellet)

Urtica urens 30C HPUS (0.44 mg)

The letters “HPUS” indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Urtica urens 30C HPUS (0.44 mg)………………Relieves itching associated with skin rash due to allergies

INDICATIONS & USAGE SECTION

Uses*

temporarily relieves itching and burning associated with minor skin irritations and rashes due to:

  • plants
  • soap
  • detergents
  • cosmetics
  • jewelry

WARNINGS SECTION

Severe Allergy Warning: Get emergency help immediately if you have rash along with any of the following symptoms:

  • trouble swallowing
  • dizziness or loss of consciousness
  • swelling of tongue
  • swelling in or around mouth
  • trouble speaking
  • drooling
  • wheezing or problems breathing

These symptoms may be signs of anaphylactic shock.

OTC - DO NOT USE SECTION

Do not use to prevent allergic skin reaction.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • persistent or severe itching
  • rash that is an unusual color, looks bruised or blistered
  • rash that does not itch
  • signs of infection (redness, warmth to the touch, severe pain, pus)

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

lactose, sucrose

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years of age and older: At the onset of symptoms, dissolve 5 pellets under the tongue every 15 minutes for 1 hour. Then, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
  • Children under 2 years of age: Ask a doctor.

OTC - QUESTIONS SECTION

BoironUSA.com

Info@Boiron.com

1-800-BOIRON-1 (1-800-264-7661)

SPL UNCLASSIFIED SECTION

  • do not use if glued carton end flaps are open or if pellet dispenser seal is broken
  • contains 0.25 g of sugar per dose
  • retain carton for full drug facts

Turn tube upside down

Twist until 5 pellets are dispensed

Remove cap and pour pellets under the tongue

SKIN ALLERGY RELIEF*

Minor Rash ▪ Burning ▪ Itching*

1 TUBE

16 DOSES PER TUBE

3 TUBES

APPROX. 80 PELLETS EACH

TOTAL 240 PELLETS

Made in France

Distributed by Boiron Inc.

Newtown Square, PA 19073

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C, K, CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-5120-41URTICA URENS30 [hp_C] in 1 TUBEPELLET303
0220-5120-43URTICA URENS30 [hp_C] in 1 TUBEPELLET303
0220-5120-43URTICA URENS3 in 1 CARTONPELLET33

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-51200220-5120-41, 0220-5120-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
URTICA URENSURTICA URENSBoiron8619a83f-7994-2de1-e053-2991aa0ae9812026-04-07WarningsExact identifier
ndc (package): 0220-5120-41
ndc (package): 0220-5120-43
ndc (product): 0220-5120
ndc11 (package): 00220512041
ndc11 (package): 00220512043
spl id: 4ee0757f-6bee-b16e-e063-6394a90a65bc
spl set id: 8619a83f-7994-2de1-e053-2991aa0ae981

Reported adverse events (FAERS/openFDA)#

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