CROMOLYN SODIUM - cromolyn sodium spray, metered 
Major Pharmaceuticals

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Cromolyn Sodium Nasal Solution USP
 NASAL SPRAY

 

(Adults and children 2 years and older)

Drug Facts

Active ingredient (per spray)

Cromolyn sodium 5.2 mg

Purpose

Nasal allergy symptom controller

Uses

to prevent and relieve nasal symptoms of hay fever and other nasal allergies:

Warnings

Do not use

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

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

Other information

Inactive ingredients

benzalkonium chloride, edetate disodium, purified water

Questions?

Serious side effects associated with use of this product may be reported to: 1-800-323-0000

Package/Label Principal Display Panel

Cromolyn Sodium Nasal Solution USP  (Carton, 26 mL - Major Pharmaceuticals)

Major

NDC 0904-5532-67

Cromolyn Sodium Nasal Solution USP

NASAL SPRAY

Nasal Allergy Symptom Controller

Prevents and Relieves Nasal Allergy Symptoms:

runny/itchy nose
sneezing
allergic stuffy nose

Without Drowsiness

Full Prescription Strength

Safe For Ages 2 Years & Older

200 Metered Sprays

Each spray delivers 5.2 mg cromolyn sodium

0.88 FL OZ (26 mL)


CROMOLYN SODIUM 
cromolyn sodium   spray, metered
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)0904-5532
Route of AdministrationNASALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CROMOLYN SODIUM (CROMOLYN) CROMOLYN SODIUM5.2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
EDETATE DISODIUM 
WATER 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
10904-5532-671 BOTTLE In 1 CARTONcontains a BOTTLE
126 mL In 1 BOTTLEThis package is contained within the CARTON (0904-5532-67)

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07570207/03/2001

Labeler - Major Pharmaceuticals (191427277)
Registrant - Bausch & Lomb Incorporated (196603781)
Establishment
NameAddressID/FEIOperations
Bausch & Lomb Incorporated807927397MANUFACTURE
Establishment
NameAddressID/FEIOperations
Aventis Pharma Manufacturing Pte LTD.595299306MANUFACTURE
Revised: 12/2010Major Pharmaceuticals