RHINOMEL MANUKA- sodium chloride spray

Rhinomel Manuka by

Drug Labeling and Warnings

Rhinomel Manuka by is a Otc medication manufactured, distributed, or labeled by Melcare Biomedical Pty Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Sodium chloride

Purpose

Nasal Wash

Uses

For persons prone to congestion

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

Directions

Adults and Children

ages over 12.

Remove cap.

Use 1-2 sprays per

nostril as needed.

Direct nozzle into your

nostril. Fully depress the

pump once or twice.

Repeat in other nostril.

After use, breathe

normally – avoid sniffing.

Wipe nozzle with clean

dry tissue after use.

Other Information

• Single patient use only.
• Discard 2 months after opening.
• Store below 25°C (77°F)

Inactive Ingredients

Water, honey (Leptospermum spp), sodium gluconate, glycerine. Preservative sodium benzoate.

Questions?

Web: www.melcare.com

Email: info@melcare.com

Phone: 855 708 2611

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RHINOMEL MANUKA 
sodium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73024-474
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	9 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BENZOATE (UNII: OJ245FE5EU)
HONEY (UNII: Y9H1V576FH)
WATER (UNII: 059QF0KO0R)
SODIUM GLUCONATE (UNII: R6Q3791S76)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73024-474-10	1 in 1 CARTON	05/21/2025
1		20 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/21/2025

Labeler - Melcare Biomedical Pty Ltd (743166886)