NASAL WASH SALINE- sodium chloride liquid 
Shenzhen Jun&Liang Media Tech Limited

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active ingredient(in each dosage unit): Sodium chloride

Purpose: Clean the nasal cavity

Uses: Work with Gailyus’s nasal washer

Warnings: Do not use with illegal drugs, alcohol, or non-prescribed medications

Ask a doctor before use:
If you have an ear infection or if your ears are blocked.
If your nasal passages are completely blocked.

Ask a doctor or pharmacist before use: if you recently had ear or nose surgery.

When using this product:
Do not use regular tap water. It recommends working with distilled, sterile or previously boiled water.

Stop use and ask a doctor if:
Your symptoms persist or worsen; or your nasal illness doesn’t improve after rinsing.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Water

Directions:
Place a new, unused saline capsule in the Gailyus nasal washer’s crushing chamber, and keep the foil-side down.
The optimal water temperature is around 35℃-40℃ (95℉-104℉) for rinsing nasal.

Questions?You can email us at Gailyus@outlook.com for more help!

Place a new, unused saline capsule in the Gailyus nasal washer’s crushing chamber, and keep the foil-side down.
The optimal water temperature is around 35℃-40℃ (95℉-104℉) for rinsing nasal.

labellabel

NASAL WASH SALINE 
sodium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83660-001
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE245 mg  in 9.5 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 7.1725 mL  in 9.5 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83660-001-1230 in 1 BOX07/28/2023
1NDC:83660-001-119.5 mL in 1 CAPSULE; Type 0: Not a Combination Product
2NDC:83660-001-2260 in 1 BOX07/28/2023
2NDC:83660-001-219.5 mL in 1 CAPSULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/28/2023
Labeler - Shenzhen Jun&Liang Media Tech Limited (444563661)
Registrant - Guangdong XINRUNTAO Technology Co., Ltd. (403789850)
Establishment
NameAddressID/FEIBusiness Operations
Guangdong XINRUNTAO Technology Co., Ltd.403789850manufacture(83660-001) , label(83660-001)

Revised: 8/2023
Document Id: 0444ce63-47de-8f99-e063-6394a90a7b4d
Set id: 0444ce63-47dd-8f99-e063-6394a90a7b4d
Version: 1
Effective Time: 20230831
 
Shenzhen Jun&Liang Media Tech Limited