Indications and uses
temporarily relieves these symptoms of hay fever or other upper respiratory allergies: nasal congestion runny nose sneezing itchy nose
McKesson Health Mart Allergy Relief
- Manufacturer
- Praxis, LLC
- Effective date
- 2023-01-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:40:10
Label at a glance#
ProductMcKesson Health Mart Allergy Relief
Active ingredientTRIAMCINOLONE ACETONIDE
Label structure9 sections
Dosage and administration
Read insert (inside package) on how to: get a new bottle ready (primed) before first use prime bottle again if not used for more than 2 weeks use the spray clean the spray nozzle ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER adults and children 12 years of age and older once daily, spray 2 times into each nostril while sniffing gently once your allergy symptoms improve, reduce to 1 spray in each nostril per day CH...
Storage and handling
do not use if printed bottle wrap is torn or opened keep package and insert. They contain important information. store between 20 o -25 o C (68 o -77 o F)
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient (in each spray)
Triamcinolone acetonide 55 mcg (glucocorticoid)
Purpose
Allergy symptom reliever
Uses
temporarily relieves these symptoms of hay fever or other upper respiratory allergies:
- nasal congestion
- runny nose
- sneezing
- itchy nose
Warnings
Do not use
- in children under 2 years of age
- if you have ever had an allergic reaction to any of the ingredients
Ask a doctor before if you
- have had recent nose ulcers or nose surgery
- have had a nose injury that has not healed
- are using a steroid medicine for asthma, allergies or skin rash
- have an eye infection
- have or had glaucoma or cataracts
When using this product
- the growth rate of some children may be slower
- some symptoms may get better on the first day of treatment. It may take up to one week of daily use to feel the most symptom relief.
- do not share this bottle with anyone else as this may spread germs
- remember to tell your doctor about all the medicines you take, including this one
Stop use and ask a doctor if
- you have, or come into contact with someone who has, chickenpox, measles or tuberculosis
- you have or develop symptoms of an infection such as a persistent fever
- you have any change in vision
- you have severe or frequent nosebleeds
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Directions
Read insert (inside package) on how to:
- get a new bottle ready (primed) before first use
- prime bottle again if not used for more than 2 weeks
- use the spray
- clean the spray nozzle
ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER | |
adults and children 12 years of age and older |
|
CHILDREN 2 TO UNDER 12 YEARS OF AGE | |
| |
children 6 to under 12 years of age |
|
children 2 to under 6 years of age |
|
children under 2 years of age |
|
| |
Other information
- do not use if printed bottle wrap is torn or opened
- keep package and insert. They contain important information.
- store between 20 o-25 oC (68 o-77 oF)
Inactive ingredients
benzalkonium chloride, carboxymethylcellulose sodium, dextrose anhydrous, edetate disodium dihydrate, hydrochloric acid or sodium hydroxide (for pH adjustment), microcrystalline cellulose, polysorbate 80, purified water
Questions or comments?
1-800-719-9260
Package/Label Principal Display Panel
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- McKesson Health Mart Allergy Relief
- Triamcinolone acetonide
- BENZALKONIUM CHLORIDE
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
- ANHYDROUS DEXTROSE
- EDETATE DISODIUM
- HYDROCHLORIC ACID
- SODIUM HYDROXIDE
- MICROCRYSTALLINE CELLULOSE
- POLYSORBATE 80
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59368-341 | 59368-341-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 31592377-da22-b387-e063-6294a90aa8ba | 3159236d-d8a0-a065-e063-6294a90afaec | 2023-01-01 | Warnings | 31592377-da22-b387-e063-6294a90aa8ba 3159236d-d8a0-a065-e063-6294a90afaec |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.