ATHOMER PROPOLIS- nasal decongestant spray

Athomer Propolis by

Drug Labeling and Warnings

Athomer Propolis by is a Otc medication manufactured, distributed, or labeled by Nobu Baby LLC, STERGIOULAS, STYLIANOS, & CO. E.E. "PHARMACOSMETIC - DIAFARM". Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Sodium Chloride (0.9%)

Purpose

Nasal decongestant

Use

• For cleaning the nasal cavity and the removal of the unpleasant mucus.
• For nasal irrigation

Directions

• For the liquidation and removal of the unpleasant mucus, apply at least 4 sprayings in each nostril up to 4 times per day
• For preventative daily use, apply 1 to 2 sprayings in each nostril every day
• Suitable for repeated long-term use
• Shake well before each use

Warnings

Use only as directed
The use of this dispenser by more than one person may spread infection
If you are pregnant or breastfeeding, seek guidance from a healthcare professional

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Other information or comments

• Store at room temperature between 68° and 77° F (20° to 25°C)

Inactive ingredients

Purified Water, Propolis

Package Label - Principal Display Panel

35 ml NDC: 80897-001-35

100 ml NDC: 80897-001-10

INGREDIENTS AND APPEARANCE

ATHOMER PROPOLIS 
nasal decongestant spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80897-001
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	0.9 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80897-001-35	35 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/04/2020
2	NDC: 80897-001-10	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/30/2020

Labeler - Nobu Baby LLC (090064974)

Establishment
Name	Address	ID/FEI	Business Operations
STERGIOULAS, STYLIANOS, & CO. E.E. "PHARMACOSMETIC - DIAFARM"		499700727	manufacture(80897-001)