HEB Anti Nausea

UNIISPLATC V06DC

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHEB

CountryUS (United States)

ATC codeV06DC

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
3780888304
1 BOTTLE in 1 CARTON (37808-883-04) / 118 mL in 1 BOTTLE

Annotations

UNII (FDA Substance ID)

IY9XDZ35W2

DEXTROSE, UNSPECIFIED FORM

RxCUI 4850

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "IY9XDZ35W2",
    "rxcui": "4850",
    "inchikey": null,
    "display_name": "DEXTROSE, UNSPECIFIED FORM",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "b76c3591-6383-4661-b3db-7a56b11202f7": {
      "match": "brand_token",
      "title": "HEB EXTRA WHITENING (FLUORIDE) PASTE, DENTIFRICE [HEB]",
      "spl_version": "15",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37808-883_403f2dcf-670b-0689-e063-6394a90ac2c7",
  "productndc": "37808-883",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROSE, UNSPECIFIED FORM; FRUCTOSE; PHOSPHORIC ACID",
  "proprietary_name": "HEB Anti Nausea",
  "active_ingred_unit": "g/5mL; g/5mL; mg/5mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Dextrose(glucose),Levulose(fructose),Phosphoric acid",
  "start_marketing_date": "20200420",
  "active_numerator_strength": "1.87; 1.87; 21.5"
}

Related drugs

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