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HEB Anti Nausea Dextrose(glucose),Levulose(fructose),Phosphoric acid 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL Liquid — NDC 37808-0883-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

HEB Anti Nausea Dextrose(glucose),Levulose(fructose),Phosphoric acid 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL Liquid — NDC 37808-883-04 (Billing 37808-0883-04) · Product 37808-883

by HEB · 1 BOTTLE in 1 CARTON (37808-883-04) / 118 mL in 1 BOTTLE

NDC 37808-883-04 (billing 37808-0883-04) is a package of HEB Anti Nausea Dextrose(glucose),Levulose(fructose),Phosphoric acid 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL Liquid from HEB, marketed since Apr 2020 and currently FDA-listed. It is the main listing for product NDC 37808-883, its only package size.

NDC 37808-0883-04
🏷️ FDA NDC (as labeled) 37808-883-04 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 37808-883-04
Product NDC 37808-883
11-digit billing NDC 37808088304
SPL Set ID fa0705c7-e50b-44bd-89ce-31b30012ab61
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-04-20
Route ORAL
Dosage form LIQUID
Substance DEXTROSE, UNSPECIFIED FORM; FRUCTOSE; PHOSPHORIC ACID
Quick answers for NDC 37808-883-04
  • 11-digit billing NDC: 37808088304
Why two NDCs? The FDA registers this code as 37808-883-04 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 37808-0883-04. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

HEB Anti Nausea is an oral liquid containing dextrose (glucose), fructose (a type of sugar), and phosphoric acid. The sugars in this product are typically used in anti-nausea formulations to provide calories and help settle an upset stomach, while phosphoric acid is commonly included in such products for its potential stomach-calming effects. This is an unapproved over-the-counter drug product.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
37808-0883-04 37808-883-04 You're viewing this Main listing 1 BOTTLE in 1 CARTON (37808-883-04) / 118 mL in 1 BOTTLE 2020-04-20 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Anti Nausea 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 00536-1302-97 RUGBY 1 bottle $0.024 — Availability likely —
Good Neighbor Anti Nausea Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 46122-0729-26 AMERISOURCE 1 bottle $0.024 — Availability likely —
Anti Nausea 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 70000-0052-01 Cardinal 1 bottle $0.024 — Availability likely —
QUALITY CHOICE Anti-Nausea 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 83324-0217-04 QUALITY 1 bottle $0.024 — Availability likely —
Walgreen Anti Nausea Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 00363-7080-04 WALGREENS 1 bottle — — FDA listed —
Walgreen Children Anti Nausea 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 00363-7081-04 WALGREENS 1 bottle — — FDA listed —
Kroger Anti Nausea Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 30142-0708-04 KROGER 1 bottle — — FDA listed —
Anti Nausea Liquid 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 36800-0708-04 TOPCO 1 bottle — — FDA listed —
HEB Anti Nausea 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mLthis 37808-0883-04 HEB 1 bottle — — FDA listed —
Meijer Anti Nausea 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 41250-0495-04 MEIJER 1 bottle — — FDA listed —
Discount Drug Mart nausea control Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 53943-0708-04 DISCOUNT 1 bottle — — FDA listed —
Anti Nausea Liquid Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 63868-0704-04 QUALITY 1 bottle — — FDA listed —
Best Choice Anti Nausea Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 63941-0708-04 BEST 1 bottle — — FDA listed —
Emetrol Cherry 1.87 g/5mL; 21.5 mg/5mL; 1.87 g/5mL 65197-0201-04 WellSpring 1 bottle — — FDA listed —
Emetrol Children Mixed Berry 1.87 g/5mL; 21.5 mg/5mL; 1.87 g/5mL 65197-0202-14 WellSpring 1 bottle — — FDA listed —
Premier Value Nausea Control Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 68016-0807-04 PHARMACY 1 bottle — — FDA listed —
CVS Anti Nausea Cherry Flavor 1.87 g/5mL; 1.87 g/5mL; 21.5 mg/5mL 69842-0708-04 CVS 1 bottle — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2020
On the market since
Apr 2020
📍
2026
Currently FDA-listed
6 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color Red
FlavorCherry
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII WZB9127XOA
    A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

4 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesFD&C Red No. 40, flavors, glycerin, methylparaben, purified water.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerHEB
Labeler code37808
First marketedApr 2020
Product typeHuman Otc Drug
Portfolio89 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

Uses for relief of upset stomach associated with nausea

⏱️ Dosage and Administration 94 words ▾

Directions for maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this product repeat dose every 15 minutes or until distress subsides do not take more than 5 doses in 1 hour without consulting a doctor measure only with dosing cup provided. Dosing cup to be used with this product only. Do not use with other products. mL= milliliter age dose adults and children 12 years of age and over 15 mL or 30 mL children 2 to under 12 years of age 5 ml or 10 mL

⚠️ Warnings 88 words ▾

Warnings this product contains fructose and should not be taken by persons with hereditary fructose intolerance (HFI). Do not use if you have allergic reactions to any of the ingredients in this product Ask a doctor before use if you have diabetes Stop use and ask a doctor if symptoms persist, return or get worse If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away at (1-800-222-1222)

🧪 Active Ingredient 17 words ▾

Active ingredients (per 5 mL) Dextrose (glucose) 1.87 g Levulose (fructose) 1.87 g Phosphoric acid 21.5 mg

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients FD&C Red No. 40, flavors, glycerin, methylparaben, purified water.

🎯 Purpose 4 words ▾

Purpose Upset Stomach Reliever

📄 Do Not Use 16 words ▾

Do not use if you have allergic reactions to any of the ingredients in this product

📄 Ask a Doctor Before Use If 9 words ▾

Ask a doctor before use if you have diabetes

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if symptoms persist, return or get worse

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 23 words ▾

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at (1-800-222-1222)

📄 Package Label / Principal Display Panel 7 words ▾

PACKAGE LABEL HEB Nausea Relief Cherry Relief

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Drug Other". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 37808-883-04, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 37808-0883-04, written without dashes as 37808088304. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 37808-0883-04, the first segment (37808) is the labeler code FDA assigned to HEB; the middle segment (0883) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (04) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by HEB. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
HEB is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 37808-0879-14 · H 37808-0886-27 · H →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.