Home NDC 69626-0084 Relief
Product NDC 69626-0084
11-digit product format 696260084
Labeler code 69626
Product ID 69626-0084_27477e10-e566-a526-e063-6394a90a7590
Type HUMAN OTC DRUG
Nonproprietary name SODIUM PHOSPHATE, MONOBASIC and SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Dosage form ENEMA
Route RECTAL
Labeler Leosons Overseas Corp
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-02-09
Substance SODIUM PHOSPHATE, MONOBASIC; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Active strength 19; 7 g/133mL; g/133mL
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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 69626-0084-6 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 69626-0084-6 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM PHOSPHATE, MONOBASIC 19 g/133mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 7 g/133mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3980JIH2SW Internal UNII lookup 70WT22SF4B Internal UNII 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 69626-0084-6 Relief 133 mL in 1 BOTTLE, WITH APPLICATOR ENEMA 133 4 69626-0084-6 Relief 1 in 1 CARTON ENEMA 1 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE ACTIVE INGREDIENT 70WT22SF4B RELIEF (SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE) ENEMA [LEOSONS OVERSEAS CORP] 1 SODIUM PHOSPHATE, MONOBASIC ACTIVE INGREDIENT 3980JIH2SW RELIEF (SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE) ENEMA [LEOSONS OVERSEAS CORP] 1 PHOSPHATE ION ACTIVE MOIETY NK08V8K8HR RELIEF (SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE) ENEMA [LEOSONS OVERSEAS CORP] 1 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 RELIEF (SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE) ENEMA [LEOSONS OVERSEAS CORP] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K RELIEF (SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE) ENEMA [LEOSONS OVERSEAS CORP] 1 WATER INACTIVE INGREDIENT 059QF0KO0R RELIEF (SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE) ENEMA [LEOSONS OVERSEAS CORP] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69626-0084 RELIEF (SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE) ENEMA [LEOSONS OVERSEAS CORP] 4 Current NDC, Legacy NDC, 2 package rows 20241121_5b301d5b-1e2c-47ed-a05f-d6be0fdfc940.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 17 of 42 · 833 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69626-0084-6 69626008406 1 BOTTLE, WITH APPLICATOR in 1 CARTON (69626-0084-6) / 133 mL in 1 BOTTLE, WITH APPLICATOR 2015-02-09 0000-00-00 No No Current