United States · FDA National Drug Code directory
HEB Anti Nausea
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 37808-883_403f2dcf-670b-0689-e063-6394a90ac2c7
- Product NDC
- 37808-883
- Form
- LIQUID
- Composition / generic term
- Dextrose(glucose),Levulose(fructose),Phosphoric acid
- Labeler
- HEB
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20200420
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROSE, UNSPECIFIED FORM — 1.87 g/5mL
- FRUCTOSE — 1.87 g/5mL
- PHOSPHORIC ACID — 21.5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (37808-883-04) / 118 mL in 1 BOTTLE · 37808-883-04
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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