OneLAX SENNA

UNIISPL

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

Identification

ManufacturerATLANTIC BIOLOGICALS CORP.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
1785611271
120 SYRINGE in 1 BOX, UNIT-DOSE (17856-1127-1) / 2.5 mL in 1 SYRINGE (17856-1127-5)
ndc11
1785611272
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1127-2) / 5 mL in 1 CUP, UNIT-DOSE (17856-1127-6)
ndc11
1785611273
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1127-3) / 10 mL in 1 CUP, UNIT-DOSE (17856-1127-7)
ndc11
1785611274
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1127-4) / 15 mL in 1 CUP, UNIT-DOSE (17856-1127-8)
ndc11
1785611279
120 SYRINGE in 1 BOX, UNIT-DOSE (17856-1127-9) / 2.5 mL in 1 SYRINGE

Annotations

UNII (FDA Substance ID)

1B5FPI42EN

SENNOSIDES A AND B

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1B5FPI42EN",
    "rxcui": null,
    "inchikey": null,
    "display_name": "SENNOSIDES A AND B",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "e6de00e6-dd81-4aab-af23-04fab261c6ff": {
      "match": "brand_token",
      "title": "ONELAX SALINE LAXATIVE (MAGNESIUM CITRATE) LIQUID [AKRON PHARMA INC]",
      "spl_version": "3",
      "published_date": "2026-01-14"
    }
  },
  "productid": "17856-1127_471b1175-9499-7889-e063-6394a90aa6dd",
  "productndc": "17856-1127",
  "dosage_form": "SYRUP",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SENNOSIDES A AND B",
  "proprietary_name": "OneLAX SENNA",
  "active_ingred_unit": "mg/237mL",
  "application_number": "M007",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "SENNA",
  "start_marketing_date": "20240206",
  "active_numerator_strength": "417.12"
}

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