FDA.reportPublic FDA data

Hive Away

Manufacturer
Feelgood Health | W. Last
Effective date
2010-08-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:02:36

Label at a glance#

ProductHive Away
Active ingredientURTICA URENS, APIS MELLIFERA, CHAMOMILE, AMMONIUM CARBONATE, TOXICODENDRON PUBESCENS LEAF
Label structure11 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Relieves hives, itching and inflammation

INDICATIONS & USAGE SECTION

Indications: Homeopathic remedy relieves hives and symptoms of poison ivy.

DOSAGE & ADMINISTRATION SECTION

Dosage: Mix 10-15 drops in ¼ cup of water and sip slowly. Repeat every 2 hours until symptoms subside. May be used with Itch Dr.™ to soothe itch.

GENERAL PRECAUTIONS SECTION

Caution: Consult your doctor if symptoms persist or worsen. Keep this and all medications out of reach of children.

OTC - ACTIVE INGREDIENT SECTION

Ingredients: Each dose contains equal parts of Urtica ur (6C) (HPUS), Apis mel (6C) (HPUS), Chamomilla (6C) (HPUS), Ammon carb (6C) (HPUS), Rhus tox (6C) (HPUS)

INACTIVE INGREDIENT SECTION

Citricidal Extract (inactive ingredient).

PREGNANCY SECTION

If pregnant or breastfeeding, ask a health professional before use.

WARNINGS SECTION

Contains no animal products, gluten, artificial flavors, preservatives or colorants. Suitable for vegetarians and safe for all ages.

INFORMATION FOR PATIENTS SECTION

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com

Distributed by

Native Remedies, LLC

6531 Park of Commerce Blvd.

Suite 160

Boca Raton, FL 33487

Phone: 1.877.289.1235

International: + 1.561.999.8857

The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopoeia of the United States.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottle labelbottle label

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of reach of children.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68647-205-102019-10-21C16284748780-1956f9ecf-de63-621f-e053-dbdaa90a74adHIVE AWAY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68647-205-10Hive Away50000 mL in 1 BOTTLE, GLASSTINCTURE500002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68647-205HIVE AWAY (URTICA UR , APIS MEL, CHAMOMILLA , AMMON CARB, RHUS TOX ) TINCTURE [FEELGOOD HEALTH]2Legacy NDC, 1 package rows20100923_704381ec-c78b-4c0b-a25d-14a4d13edbed.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMMONIUM CARBONATEACTIVE INGREDIENTNJ5VT0FKLJ2
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z2
CHAMOMILEACTIVE INGREDIENTFGL3685T2X2
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A2
URTICA URENSACTIVE INGREDIENTIHN2NQ5OF92
AMMONIUM CATIONACTIVE MOIETY54S68520I42
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z2
CHAMOMILEACTIVE MOIETYFGL3685T2X2
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A2
URTICA URENSACTIVE MOIETYIHN2NQ5OF92
CITRUS PARADISI SEEDINACTIVE INGREDIENT12F08874Y72
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68647-20568647-205-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
URTICA URENSIHN2NQ5OF9ACTIB
APIS MELLIFERA7S82P3R43ZACTIB
CHAMOMILEFGL3685T2XACTIB
AMMONIUM CARBONATENJ5VT0FKLJACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
CITRUS PARADISI SEED12F08874Y7IACT
WATER059QF0KO0RIACT

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
ddea6f89-5da8-4f02-8edd-3a5944be2fed704381ec-c78b-4c0b-a25d-14a4d13edbed2010-08-16WarningsExact identifier
spl id: ddea6f89-5da8-4f02-8edd-3a5944be2fed
spl set id: 704381ec-c78b-4c0b-a25d-14a4d13edbed

Reported adverse events (FAERS/openFDA)#

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