ZICAM ALLERGY RELIEF- galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, and sulfur spray
Matrixx Initiatives, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Zicam® Allergy Relief Nasal Gel

Drug Facts

Active ingredients

Galphimia glauca 12x, 30x
Histaminum hydrochloricum 12x, 30x, 200x
Luffa operculata 4x, 12x, 30x
Sulphur 12x, 30x, 200x

Purpose

Upper respiratory allergy symptom relief

Uses

temporarily relieves symptoms due to hay fever or other upper respiratory allergies such as:
- sinus pressure
- itchy, runny nose
- sneezing
- itchy, watery eyes
- nasal congestion

Warnings

For nasal use only.

Ask a doctor before use if you have

ear, nose, or throat sensitivity
susceptibility to nosebleeds
breathing problems such as emphysema or chronic bronchitis

When using this product

avoid contact with eyes. Rinse right away with water if it gets in eyes and seek medical help right away.
the use of this container by more than one person may spread infection
temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge may occur

Stop use and ask a doctor if symptoms persist or are accompanied by fever

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 12 years of age and older:
- remove cap and safety clip (also see illustrations on side of carton)
- hold with thumb at bottom of bottle and nozzle between your fingers
- before using the first time, prime pump by depressing several times
- place tip of nozzle just past nasal opening (approximately 1/8")
- while inside nasal opening, slightly angle nozzle outward
- pump once into each nostril
- after application, press lightly on outside of each nostril for about 5 seconds
- wait at least 30 seconds before blowing nose
use once every 4 hours
optimal results may not be seen for 1-2 weeks. After 1-2 weeks, you may need to use only 1-2 times daily. For best results, use up to 1 week before contact with known causes of your allergies.
children under 12 years of age: ask a doctor

Other information

store between 15-29°C (59-84°F)

Inactive ingredients

benzalkonium chloride, benzyl alcohol, edetate disodium, glycerin, hydroxyethylcellulose, potassium chloride, potassium phosphate, purified water, sodium chloride, sodium phosphate

Questions? Comments? Side Effects?

call 877-942-2626 toll free

Distributed by Matrixx Initiatives, Inc.
Scottsdale, Arizona 85260.

PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton

NDC 62750-001-11

ZICAM®

POWERFUL
ALLERGY
RELIEF

HOMEOPATHIC
• #1 •
ALLERGY BRAND*

No-Drip Liquid®
NASAL SPRAY

Effective Non-Drowsy Relief of:

Runny Nose
Watery Eyes
Itchy Nose
Sneezing

No Known Allergy Drug Interactions

0.50 FL OZ (15 mL)
HOMEOPATHIC

Principal Display Panel - 15 mL Bottle Carton

ZICAM ALLERGY RELIEF
galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, and sulfur spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:62750-001
Route of Administration	NASAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
galphimia glauca flowering top (UNII: 93PH5Q8M7E) (galphimia glauca flowering top - UNII:93PH5Q8M7E)	galphimia glauca flowering top	30 [hp_X] in 1 mL
histamine dihydrochloride (UNII: 3POA0Q644U) (histamine - UNII:820484N8I3)	histamine dihydrochloride	200 [hp_X] in 1 mL
luffa operculata fruit (UNII: C4MO6809HU) (luffa operculata fruit - UNII:C4MO6809HU)	luffa operculata fruit	30 [hp_X] in 1 mL
sulfur (UNII: 70FD1KFU70) (sulfur - UNII:70FD1KFU70)	sulfur	200 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
benzalkonium chloride (UNII: F5UM2KM3W7)
benzyl alcohol (UNII: LKG8494WBH)
edetate disodium (UNII: 7FLD91C86K)
glycerin (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
potassium chloride (UNII: 660YQ98I10)
potassium phosphate, unspecified form (UNII: B7862WZ632)
water (UNII: 059QF0KO0R)
sodium chloride (UNII: 451W47IQ8X)
sodium phosphate (UNII: SE337SVY37)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:62750-001-11	1 in 1 CARTON	04/14/2000	10/31/2023
1		15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC:62750-001-12	1 in 1 CARTON	04/14/2000	10/31/2023
2		30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
UNAPPROVED HOMEOPATHIC		04/14/2000	10/31/2023

Labeler - Matrixx Initiatives, Inc. (790037253)

Name	Address	ID/FEI	Business Operations
Establishment
Accupac, Inc.		071609663	MANUFACTURE(62750-001)

Revised: 1/2022

Document Id: d704726f-b472-486c-9ac7-d89df9795bd3

Set id: 04d551dc-23f9-414b-aac4-e92d111c867d

Version: 6

Effective Time: 20220125

Matrixx Initiatives, Inc.