Home NDC 70708-110 GURUNANDA NASAL SALINE
Product NDC 70708-110
11-digit product format 707080110
Labeler code 70708
Product ID 70708-110_40ab4164-135d-b935-e063-6294a90acb33
Type HUMAN OTC DRUG
Nonproprietary name NASAL WASH
Dosage form POWDER, FOR SOLUTION
Route NASAL
Labeler GURUNANDA LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2024-02-12
Substance SODIUM BICARBONATE; SODIUM CHLORIDE
Active strength .515; 1.685 g/2.2g; g/2.2g
Pharmacologic classes Alkalinizing Activity [MoA], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base GURUNANDA NASAL SALINE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE .515 g/2.2g SODIUM CHLORIDE 1.685 g/2.2g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8MDF5V39QO Internal UNII lookup 451W47IQ8X Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1804375 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70708-110-12 GURUNANDA NASAL SALINE 2.2 g in 1 PACKET POWDER, FOR SOLUTION 2.2 2 70708-110-12 GURUNANDA NASAL SALINE 120 in 1 BOX POWDER, FOR SOLUTION 120 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70708-110 GURUNANDA NASAL SALINE (NASAL WASH) POWDER, FOR SOLUTION [GURUNANDA LLC] 1 Current NDC, 2 package rows 20250112_2b4d78ae-b587-6dfe-e063-6394a90a8876.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70708-110-12 70708011012 120 PACKET in 1 BOX (70708-110-12) / 2.2 g in 1 PACKET 120 packet 2024-02-12 No No Current