Home NDC 41520-938-50 All natural Saline Packets
Product NDC 41520-938
Requested package NDC 41520-938-50
11-digit product format 415200938
Labeler code 41520
Product ID 41520-938_459bb460-21c3-9c34-e063-6294a90afba3
Type HUMAN OTC DRUG
Nonproprietary name SODIUM BICARBONATE, SODIUM CHLORIDE
Dosage form POWDER, FOR SOLUTION
Route NASAL
Labeler FOODHOLD U.S.A.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2022-01-08
Substance SODIUM BICARBONATE; SODIUM CHLORIDE
Active strength 700; 2300 mg/3000mg; mg/3000mg
Pharmacologic classes Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 41520-938 41520-938-50 I Inactivated by FDA excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 41520-938 41520-938-50 I Inactivated by FDA excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Additional Listing Data#
Finished product Yes
Brand name base All natural Saline Packets
Brand name suffix CareOne
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 700 mg/3000mg SODIUM CHLORIDE 2300 mg/3000mg
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 1542919 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41520-938-50 All natural Saline PacketsCareOne 50 in 1 CARTON POWDER, FOR SOLUTION 50 3 41520-938-50 All natural Saline PacketsCareOne 3000 mg in 1 PACKET POWDER, FOR SOLUTION 3000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41520-938 ALL NATURAL SALINE PACKETS CAREONE (SODIUM BICARBONATE, SODIUM CHLORIDE) POWDER, FOR SOLUTION [FOODHOLD U.S.A.] 2 Current NDC, Legacy NDC, 2 package rows 20240118_e32f105d-65cd-8095-e053-2995a90a9b6b.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 Marketing end Sample Exclude flag Status 41520-938-50 41520093850 50 PACKET in 1 CARTON (41520-938-50) / 3000 mg in 1 PACKET 50 packet 2022-01-08 0000-00-00 No No Current