Hives

Manufacturer
Natural Creations, Inc | OHM Pharma, Inc
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:36:00

Label at a glance#

ProductHives
Active ingredientECHINACEA ANGUSTIFOLIA WHOLE, APIS MELLIFERA, ARSENIC TRIOXIDE, PHENOL, RHODODENDRON TOMENTOSUM LEAFY TWIG, TOXICODENDRON PUBESCENS LEAF, SULFUR, URTICA URENS WHOLE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (*HPUS) - equal amounts of: Echinacea Ang 4X, Apis Mel 12X, Arsenicum Alb 12X, Carbolicum Ac 12X, Ledum 12X, Rhus Tox 12X, Sulphur 12X, Urtica Urens 12X

INDICATIONS & USAGE SECTION

USES: Temporarily relieves itching, burning, rosy or red skin.**

OTC - PURPOSE SECTION

USES: Temporarily relieves itching, burning, rosy or red skin.**

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

WARNINGS:

  • Consult a physician for use in children under 12 years of age.
  • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
  • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
  • Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

REFERENCES SECTION

*The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:43406-0691-1

Hives

HOMEOPATHIC

1 fl oz (30mL) / 20% Alcohol

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730001580GTIN-13: 0877730001580
EAN-13: 0877730001580
GTIN-12: 877730001580
UPC-A: 877730001580
GTIN storage (14 digits): 00877730001580
Hives.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0691-1Hives30 mL in 1 BOTTLE, DROPPERLIQUID302

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-069143406-0691-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
HivesECHINACEA ANG, APIS MEL, ARSENICUM ALB, CARBOLICUM AC, LEDUM, RHUS TOX, SULPHUR, URTICA URENSNatural Creations, Incc453ac40-1865-4297-b7d4-c8e637bb5f942025-12-16WarningsExact identifier
ndc (package): 43406-0691-1
ndc (product): 43406-0691
ndc11 (package): 43406069101
spl id: 970a2cc0-5218-4600-bb50-4584fd1b63c3
spl set id: c453ac40-1865-4297-b7d4-c8e637bb5f94

Reported adverse events (FAERS/openFDA)#

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