Home NDC 70708-210 GURUNANDA NASAL SALINE
Product NDC 70708-210
11-digit product format 707080210
Labeler code 70708
Product ID 70708-210_434867fa-398a-2418-e063-6394a90afd51
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 70708-210-08 GURUNANDA NASAL SALINE 8 in 1 BOX POWDER, FOR SOLUTION 8 2 70708-210-08 GURUNANDA NASAL SALINE 2.2 g in 1 PACKET POWDER, FOR SOLUTION 2.2 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70708-210 GURUNANDA NASAL SALINE (NASAL WASH) POWDER, FOR SOLUTION [GURUNANDA LLC] 1 Current NDC, 2 package rows 20241129_27dbf0bf-c273-2108-e063-6394a90a0a09.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 70708-210-08 70708021008 8 PACKET in 1 BOX (70708-210-08) / 2.2 g in 1 PACKET 8 packet 2024-02-12 No No Current