Manuka Honey Extra Strength

UNIISPL

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

Identification

ManufacturerFirst Honey LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8199505001
1 TUBE in 1 CARTON (81995-050-01) / 21 g in 1 TUBE

Annotations

UNII (FDA Substance ID)

344S277G0Z

ALLANTOIN

RxCUI 508

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "b742585d-9a0c-489b-b268-590583cfabd1": {
      "match": "brand_token",
      "title": "MANUKA HONEY EXTRA STRENGTH (ALLANTOIN) GEL [FIRST HONEY LLC]",
      "spl_version": "3",
      "published_date": "2025-02-06"
    }
  },
  "productid": "81995-050_2d5e1f54-b018-fce5-e063-6394a90a76d7",
  "productndc": "81995-050",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "Manuka Honey Extra Strength",
  "active_ingred_unit": "mg/g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "ALLANTOIN",
  "start_marketing_date": "20240901",
  "active_numerator_strength": "5"
}

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