Home NDC 67234-041-01 ORAL SALINE LAXATIVE CHERRY
Product NDC 67234-041
Requested package NDC 67234-041-01
11-digit product format 672340041
Labeler code 67234
Product ID 67234-041_214096c4-abf7-4d4f-b93b-6a0a2f3b7c15
Type HUMAN OTC DRUG
Nonproprietary name SODIUM PHOSPHATE, DIBASIC and SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM
Dosage form LIQUID
Route ORAL
Labeler Natureplex, LLC
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2012-08-31
Marketing end 0000-00-00
Substance SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM; SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM
Active strength 1 g/14.7868mL; g/14.7868mL
NDC exclude flag No
Listing certified through 2020-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 67234-041-01 ORAL SALINE LAXATIVE CHERRY LAXATIVE 1 in 1 CARTON LIQUID 1 3 67234-041-01 ORAL SALINE LAXATIVE CHERRY LAXATIVE 45 mL in 1 BOTTLE LIQUID 45 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67234-041 ORAL SALINE LAXATIVE CHERRY LAXATIVE (SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM) LIQUID [NATUREPLEX, LLC] 3 Legacy NDC, 2 package rows 20180616_b079c681-fc8e-416e-ba50-51091efe36c7.zip
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 67234-041-01 67234004101 1 BOTTLE in 1 CARTON (67234-041-01) > 45 mL in 1 BOTTLE 1 bottle 2012-08-31 0000-00-00 No No Current