FDA.reportPublic FDA data

Nature Knows Allergy Relief

Manufacturer
NaturoDRJ Enterprises | OHM PHARMA INC.
Effective date
2017-11-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:57

Label at a glance#

ProductNature Knows Allergy Relief
Active ingredientONION, AMBROSIA ARTEMISIIFOLIA, ARALIA RACEMOSA ROOT, JACOBAEA MARITIMA, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, NAPHTHALENE, POPULUS BALSAMIFERA LEAF BUD, QUERCUS ROBUR NUT, SALIX NIGRA BARK, SAMBUCUS NIGRA FLOWERING TOP, THUJA OCCIDENTALIS LEAFY TWIG, ULMUS MINOR FLOWERING TWIG, URTICA URENS, ANTHOXANTHUM ODORATUM, CANDIDA ALBICANS
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of:

Allium Cepa 10X, 30X; Ambrosia Artemisiaefolia 10X, 30X; Aralia Racemosa 10X, 30X; Cineraria Maritima 10X, 30X; Histaminum Hydrochloricum 10X, 30X; Luffa Operculata 10X, 30X; Naphthalinum 10X, 30X; Populus Candicans 10X, 30X; Quercus Glandium Spiritus 10X, 30X; Salix Nigra 10X, 30X; Sambucus Nigra 10X, 30X; Thuja Occidentalis 10X, 30X; Ulmus Procera, Flos 10X, 30X; Urtica Urens 10X 30X; Anthoxanthum 15X, 30X; Candida Albicans 15X, 30X.

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

INDICATIONS & USAGE SECTION

USES:

For temporary relief of watery eyes, runny nose and scratchy throat due to exposure of allergens.**

​**This statement has not been evaluated by the FDA, it is based on documented Homeopathic Materia Medica.

WARNINGS SECTION

WARNINGS:

  • If symptoms worsen or persist for more than 10 days, discontinue use and consult your health care professional.
  • If pregnant or breast-feeding, or have a known medical condition, consult a physician before use. 
  • Keep out of reach of children.
  • In case of overdose, get medical help or contact a poison control center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS:

Adults and children 12 and older, ten (10) drops under the tongue three (3) times a day or until symptoms are relieved. Take only when needed. Consult a physician for use in children under 12 years of age. Do not eat or drink for at least 15 minutes before or after dose.

OTHER SAFETY INFORMATION

OTHER INFORMATION:

  • Do not use if tamper evident seal is broken or missing.
  • Store at room temperture away from direct sunlight and moisture.

INACTIVE INGREDIENT SECTION

​INACTIVE INGREDIENTS:

Ethyl alcohol USP, Purified water.

OTC - QUESTIONS SECTION

​Manufactured for:

Naturodrj Enterprises

Austin, TX 78735

24/7 Toll Free: (800) 396-2120

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Homeopathic Formula

Nature Knows

Allergy Relief

Net 2 fl oz (59 ml) - contains 20% alcohol

www.TexasKnowsAllergy.com

Professional Strength

Made in America

2oz bottle label2oz bottle label

OTC - PURPOSE SECTION

Allergy Relief

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71559-301-022020-01-31C16284748780-19d75b9cf-dcd6-f424-e053-dadaa90a57ceNature Knows Allergy Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71559-301-02Nature Knows Allergy Relief59 mL in 1 BOTTLE, DROPPERLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71559-301NATURE KNOWS ALLERGY RELIEF (ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARALIA RACEMOSA, CINERARIA MARITIMA, HISTAMINUM HYDROCHLORICUM, LUFFA OPERCULATA, NAPHTHALINUM, POPULUS CANDICANS, QUERCUS GLANDIUM SPIRITUS, SALIX NIGRA, SAMBUCUS NIGRA, THUJA OCCIDENTALIS, ULMUS PROCERA FLOS, URTICA URENS, ANTHOXANTHUM, CANDIDA ALBICANS.) LIQUID [NATURODRJ ENTERPRISES]1Legacy NDC, 1 package rows20171102_e38a3a25-5554-4483-8743-903b7b451c15.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71559-30171559-301-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ONION492225Q21HACTIB
AMBROSIA ARTEMISIIFOLIA9W34L2CQ9AACTIB
ARALIA RACEMOSA ROOTT90W4582DUACTIB
JACOBAEA MARITIMAU4B223LS4XACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
LUFFA OPERCULATA FRUITC4MO6809HUACTIB
NAPHTHALENE2166IN72UNACTIB
POPULUS BALSAMIFERA LEAF BUD9CQ6C00G3CACTIB
QUERCUS ROBUR NUTQ7MU1F4GLYACTIB
SALIX NIGRA BARKQU52J3A5B3ACTIB
SAMBUCUS NIGRA FLOWERING TOPCT03BSA18UACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
ULMUS MINOR FLOWERING TWIGJ3O020I532ACTIB
URTICA URENSIHN2NQ5OF9ACTIB
ANTHOXANTHUM ODORATUMYMW1K70E4QACTIB
CANDIDA ALBICANS4D7G21HDBCACTIB
ALCOHOL3K9958V90MIACT
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
58990631-b2a0-45b0-bf84-00dac9d987a9e38a3a25-5554-4483-8743-903b7b451c152017-11-01WarningsExact identifier
spl id: 58990631-b2a0-45b0-bf84-00dac9d987a9
spl set id: e38a3a25-5554-4483-8743-903b7b451c15

Reported adverse events (FAERS/openFDA)#

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