Cleanoz description, usages, side effects, indications, overdosage, supplying and lots more!

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Cleanoz

Laboratoires Gifrer Barbezat


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Cleanoz Uses

  • Recommended for nasal rinsing in babies, children and adults.
Recommended for the following cases:
  • Hygiene of nasal passage: Pollution, dry air, airconditioning, dust, pollen.
  • Moisture efficiency.
  • Nasal drainage. For babies and infants, this can be assisted with the use of Cleanoz® nasal aspirator kitTM

Warning

For external use only, do not inject

  • Do not use if solution changes color or becomes cloudy.

When using this product

  • Use only if applicator is intact.
  • To avoid contamination, do not touch tip of the container to any surface.
  • Do not reuse. Once opened, discard.
  • Do not use the same applicator on different people.

Keep out of reach of children.

Direction

  • Twist and pull tab to remove.
  • Tilt on the applicator to obtain the necessary dosage.
  • Directions for use for babies and infants: Place the baby with its head leaning to the side. Place carefully the tip of the applicator in one nostril. Tilt to obtain the necessary dosage. Repeat on the other nostril.
  • Use as often as needed for any length of time or as directed by physician. Non habit forming.
Other information
  • Store at 68-77°F (20-25°C).
  • Retain this carton for future reference.
  • Use before expiration date marked on the carton or containers.

Inactive ingredients

Purified water, 0.9% Sodium Chloride

Questions?   1-866-5-UBIMED   info@ubimed.com

Principal Display Panel

Cleanoz(R)

Saline solution

Natural relief for dry or stuffy noses

Convenient and hygienic

Newborns to adults

The #1 Choice of Healthcare Professionals

Preservative-free vials

Ubimed

3/5/10/20/30/40 Count

3/5/10/20/30/40 Sterile Single-Use Applicators

5mL (0.169 FL OZ) Each

Cleanoz

Cleanoz

sodium chloride SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:44929-002
Route of Administration NASAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE 900 mg

Inactive Ingredients

Ingredient Name Strength
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:44929-002-01 5 in 1 AMPULE
2 NDC:44929-002-01 5 in 1 AMPULE
3 NDC:44929-002-01 5 in 1 AMPULE
4 NDC:44929-002-01 5 in 1 AMPULE
5 NDC:44929-002-01 5 in 1 AMPULE
6 NDC:44929-002-01 5 in 1 AMPULE
7 NDC:44929-002-07 30 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2008-11-25


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