FDA.reportPublic FDA data

HEB Anti Nausea

Product NDC
37808-883
11-digit product format
378080883
Labeler code
37808
Product ID
37808-883_403f2dcf-670b-0689-e063-6394a90ac2c7
Type
HUMAN OTC DRUG
Nonproprietary name
Dextrose(glucose),Levulose(fructose),Phosphoric acid
Dosage form
LIQUID
Route
ORAL
Labeler
HEB
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-04-20
Substance
DEXTROSE, UNSPECIFIED FORM; FRUCTOSE; PHOSPHORIC ACID
Active strength
1.87; 1.87; 21.5 g/5mL; g/5mL; mg/5mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
HEB Anti Nausea
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DEXTROSE, UNSPECIFIED FORM1.87 g/5mL
FRUCTOSE1.87 g/5mL
PHOSPHORIC ACID21.5 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
IY9XDZ35W2Internal UNII lookup
6YSS42VSEVInternal UNII lookup
E4GA8884NNInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
318146Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
fa0705c7-e50b-44bd-89ce-31b30012ab61Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-883-04HEB Anti Nausea1 in 1 CARTONLIQUID18
37808-883-04HEB Anti Nausea118 mL in 1 BOTTLELIQUID1188

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-883HEB ANTI NAUSEA (DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID) LIQUID [HEB]7Current NDC, Legacy NDC, 2 package rows20240915_fa0705c7-e50b-44bd-89ce-31b30012ab61.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HEB Anti NauseaDEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACIDHEBfa0705c7-e50b-44bd-89ce-31b30012ab612025-10-03WarningsExact identifier
ndc (product): 37808-883

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG in 5 mL Oral SolutionPSNfa0705c7-e50b-44bd-89ce-31b30012ab618
318146fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral SolutionSCDfa0705c7-e50b-44bd-89ce-31b30012ab618
318146dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral SolutionSYfa0705c7-e50b-44bd-89ce-31b30012ab618

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37808-883-04378080883041 BOTTLE in 1 CARTON (37808-883-04) / 118 mL in 1 BOTTLE1 bottle2020-04-200000-00-00NoNoCurrent