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

Zicam Allergy Relief by

Drug Labeling and Warnings

Zicam Allergy Relief by is a Homeopathic medication manufactured, distributed, or labeled by Matrixx Initiatives, Inc., Accupac, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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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

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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

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

Inactive Ingredients
Ingredient Name	Strength
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)

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

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

Labeler - Matrixx Initiatives, Inc. (790037253)

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