Nasal Decongestant

Manufacturer
Natural Creations, Inc | OHM Pharma, Inc
Effective date
2018-12-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:19:28

Label at a glance#

ProductNasal Decongestant
Active ingredientCAMELLIA SINENSIS WHOLE, EPHEDRA DISTACHYA FLOWERING TWIG, ATROPA BELLADONNA, ARSENIC TRIOXIDE, MERCURIC SULFIDE, POTASSIUM DICHROMATE, PULSATILLA VULGARIS WHOLE, SEPIA OFFICINALIS JUICE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, MERCURIUS SOLUBILIS, SULFUR
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS - equal amounts of: Camellia Sinensis 4X, Ephedra Vulgaris 4X, Belladonna 4X, Arsenicum Album 12X, Cinnabaris 12X, Kali Bichromicum 12X, Pulsatilla 12X, Sepia 12X, Calcarea Carbonica 30X, Mercurius Solubilis 30X, Sulphur 30X

INDICATIONS & USAGE SECTION

USES: Temporary relief of nasal congestion.**

OTC - PURPOSE SECTION

USES: Temporary relief of nasal congestion.**

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

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:43406-0693-1

Nasal Decongestant

HOMEOPATHIC

1 fl oz (30mL) / 20% Alcohol

image descriptionimage description

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
43406-0693-1Nasal Decongestant30 mL in 1 BOTTLE, DROPPERLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0693NASAL DECONGESTANT (CAMELLIA SINENSIS, EPHEDRA VULGARIS, BELLADONNA, ARSENICUM ALBUM, CINNABARIS, KALI BICHROMICUM, PULSATILLA, SEPIA, CALCAREA CARBONICA, MERCURIUS SOLUBILIS, SULPHUR) LIQUID [NATURAL CREATIONS, INC]1Current NDC, Legacy NDC, 1 package rows20230111_938a25f8-e854-4537-a04d-5e2276199f5c.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-069343406-0693-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
Nasal DecongestantCAMELLIA SINENSIS, EPHEDRA VULGARIS, BELLADONNA, ARSENICUM ALBUM, CINNABARIS, KALI BICHROMICUM, PULSATILLA, SEPIA, CALCAREA CARBONICA, MERCURIUS SOLUBILIS, SULPHURNatural Creations, Inc938a25f8-e854-4537-a04d-5e2276199f5c2018-12-21WarningsExact identifier
ndc (package): 43406-0693-1
ndc (product): 43406-0693
ndc11 (package): 43406069301
spl id: f488ac0b-aa2f-4b24-850a-1898ed7930d3
spl set id: 938a25f8-e854-4537-a04d-5e2276199f5c

Reported adverse events (FAERS/openFDA)#

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