FAMILY CARE NASAL RELIEF - oxymetazoline hydrochloride spray 
United Exchange Corp

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient                                                                                 Purpose

Oxymetazoline HCl 0.05%.................................................Nasal Decongestant

Uses

Warnings For nasal use only

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if symptoms persist

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, benzyl alcohol, dibasic sodium phosphate hydrate, disodium EDTA, distilled water, monobasic sodium phosphate dihydrate, PEG 1450, PVP K30

Distributed By:

United Exchange Corp

17211 Valley View Ave.

Cerritos, CA 90703 USA

Made in Korea

image of carton label

FAMILY CARE NASAL RELIEF 
oxymetazoline hydrochloride spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:65923-551
Route of Administration NASAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE 0.05 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)  
POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)  
POVIDONE K30 (UNII: U725QWY32X)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65923-551-30 1 in 1 CARTON
1 30 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 06/30/2013
Labeler - United Exchange Corp (840130579)

Revised: 6/2013
Document Id: c4e866a6-8dd7-4695-97a0-5daccbe34f55
Set id: a420da2c-5aa8-4398-acee-412c1dc346bb
Version: 1
Effective Time: 20130630
 
United Exchange Corp