ANCIENT SECRETS  BREATHE AGAIN- sodium chloride aerosol, spray 
LOTUS BRANDS, INC.

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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ANCIENT
SECRETS®
Breathe
Again™
Hypertonic Seawater
Nasal Spray

Drug Facts

Active ingredient

Sodium Chloride 2.0% (Seawater-derived)

Purpose

Restores Moisture

Uses

for nasal rinsing in adults:

Warnings

For nasal use only.

When using this product

  • To avoid contamination, do not touch tip of the dispenser to any surface.
  • Do not use the same dispenser on different people.

Stop use and ask a doctor if you experience any discomfort while using this product.

Keep out of the reach of children.

Directions

Other Information

Inactive Ingredients

purified water

Questions, Comments, Side Effects?

Call toll free 800-824-6396, Monday – Friday, 9:00 – 5:00, CST

Manufactured by
Gerolymatos International S.A.
Athens, Greece

®©2011, Distributed by Lotus Brands, Inc.,
A majority woman-owned family business
1100 Lotus Drive, Silver Lake, WI 53170, USA

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton

ANCIENT
SECRETS
®

Breathe
Again™

Hypertonic Seawater
Nasal Spray

3.38 fl.oz. (100 mL)

Principal Display Panel - 100 mL Bottle Carton
ANCIENT SECRETS   BREATHE AGAIN
sodium chloride aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76328-100
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Chloride (UNII: 451W47IQ8X) (Sodium Cation - UNII:LYR4M0NH37) Sodium Chloride20 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76328-100-001 in 1 CARTON08/15/2011
1100 mL in 1 CANISTER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34908/15/2011
Labeler - LOTUS BRANDS, INC. (879022713)
Establishment
NameAddressID/FEIBusiness Operations
GEROLYMATOS INTERNATIONAL SA506173753MANUFACTURE(76328-100)

Revised: 10/2018
Document Id: fe980cd8-fb02-4042-881e-cdf30fbf2d6d
Set id: c6d2bab0-d363-4c09-a71b-ae15db915b37
Version: 2
Effective Time: 20181030
 
LOTUS BRANDS, INC.