Rhinomel Manuka

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Rhinomel Manuka
Generic name
SODIUM CHLORIDE
Manufacturer
Melcare Biomedical Pty Ltd
Product type
HUMAN OTC DRUG
SPL set ID
35a7ce7d-4a26-e3f0-e063-6294a90ad66f
SPL ID
458a65a1-575a-a14d-e063-6294a90ace39
Version
2
Effective date
2025-12-09
Source export date
2026-10-30
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:58:47
Harmonized routes table
Harmonized routes
NASAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings • Do not use if hyper-sensitive to bee products, pollens or the preservative benzoic acid; • Not suitable for persons with irritated nasal linings or suspected sinus infection. The natural acidity of honey may result in transient discomfort; • For any reaction other than transient discomfort cease use and contact your health care professional; • Consult your doctor if symptoms persist for more than 1 week, tend to reoccur or are accompanied by pain or a persistent headache. These could be signs of a serious condition; • Not recommended for pregnant women or children under 12 years without medical advice; • Replace cap after use; • Do not use if packaging is damaged or carton tamper seal is broken before first use. • Keep out of reach of children

Reported adverse events (FAERS/openFDA)#

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