Home NDC 71753-8010 Natrum Phosphoricum
Product NDC 71753-8010
11-digit product format 717538010
Labeler code 71753
Product ID 71753-8010_f8f8d698-66d8-409e-a9f9-38118cb3fc7a
Type HUMAN OTC DRUG
Nonproprietary name Natrum Phosphoricum
Dosage form SPRAY
Route ORAL
Labeler Ratis, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-09-30
Marketing end 2025-10-26
Substance SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Active strength 6 [hp_X]/mL
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record 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 product product 71753-8010 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 71753-8010 71753-8010-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Product Concepts# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71753-8010 NATRUM PHOSPHORICUM SPRAY [RATIS, LLC] 2 Legacy NDC 20220121_3b808bfc-551a-4561-ab11-2f91e030aef7.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71753-8010-1 71753801001 30 mL in 1 BOTTLE, SPRAY (71753-8010-1) 30 ml 2020-09-30 0000-00-00 No No Current