Home NDC 49348-576-27 sunmark anti nausea
Product NDC 49348-576
Requested package NDC 49348-576-27
11-digit product format 493480576
Labeler code 49348
Product ID 49348-576_bc2d9312-7217-4d73-ba6e-c87d43d58c9d
Type HUMAN OTC DRUG
Nonproprietary name Dextrose (glucose), Levulose (fructose), Phosphoric Acid
Dosage form SOLUTION
Route ORAL
Labeler Strategic Sourcing Services LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2003-10-07
Marketing end 2023-01-31
Substance DEXTROSE, UNSPECIFIED FORM; FRUCTOSE; PHOSPHORIC ACID
Active strength 2 g/5mL; g/5mL; mg/5mL
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DEXTROSE ACTIVE INGREDIENT IY9XDZ35W2 SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 FRUCTOSE ACTIVE INGREDIENT 6YSS42VSEV SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 PHOSPHORIC ACID ACTIVE INGREDIENT E4GA8884NN SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 DEXTROSE ACTIVE MOIETY IY9XDZ35W2 SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 FRUCTOSE ACTIVE MOIETY 6YSS42VSEV SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 PHOSPHORIC ACID ACTIVE MOIETY E4GA8884NN SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2 WATER INACTIVE INGREDIENT 059QF0KO0R SUNMARK ANTI NAUSEA (DEXTROSE (GLUCOSE), LEVULOSE (FRUCTOSE), PHOSPHORIC ACID) LIQUID [MCKESSON] 2
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49348-576-27 49348057627 1 BOTTLE in 1 CARTON (49348-576-27) > 118 mL in 1 BOTTLE 1 bottle 2003-10-07 2023-01-31 No No Current