Kesin MAG-AL

UNIISPL

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

Identification

ManufacturerKesin Pharma Corporation

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8103300501
100 CUP, UNIT-DOSE in 1 CASE (81033-005-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-005-30)

Annotations

UNII (FDA Substance ID)

5QB0T2IUN0

ALUMINUM HYDROXIDE

RxCUI 81948

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "5QB0T2IUN0",
    "rxcui": "81948",
    "inchikey": "WNROFYMDJYEPJX-UHFFFAOYSA-K",
    "display_name": "ALUMINUM HYDROXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "436b622a-f028-df98-e063-6394a90a3eaa": {
      "match": "brand_token",
      "title": "KESIN MAG-AL PLUS (ALUMINUM AND MAGNESIUM HYDROXIDE W/SIMETHICONE SUSPENSION) SUSPENSION [KESIN PHARMA CORPORATION]",
      "spl_version": "2",
      "published_date": "2026-05-13"
    }
  },
  "productid": "81033-005_515188f8-2cea-822a-e063-6394a90a3a2c",
  "productndc": "81033-005",
  "dosage_form": "SUSPENSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE",
  "proprietary_name": "Kesin MAG-AL",
  "active_ingred_unit": "mg/5mL; mg/5mL",
  "application_number": "M001",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Aluminum and Magnesium Hydroxide Suspension",
  "start_marketing_date": "20251105",
  "active_numerator_strength": "200; 200"
}

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