CITRUCEL

UNIISPL

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

Identification

ManufacturerHaleon US Holdings LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
0135019901
180 TABLET in 1 BOTTLE (0135-0199-01)
ndc11
0135019902
100 TABLET in 1 BOTTLE (0135-0199-02)
ndc11
0135019906
2 TABLET in 1 POUCH (0135-0199-06)
ndc11
0135019907
240 TABLET in 1 BOTTLE (0135-0199-07)
ndc11
0135019908
50 POUCH in 1 CARTON (0135-0199-08) / 2 TABLET in 1 POUCH (0135-0199-06)
ndc11
0135019909
1 BOTTLE in 1 PACKAGE (0135-0199-09) / 240 TABLET in 1 BOTTLE

Annotations

UNII (FDA Substance ID)

MRJ667KA5E

METHYLCELLULOSE (4000 MPA.S)

RxCUI 1297402

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "MRJ667KA5E",
    "rxcui": "1297402",
    "inchikey": null,
    "display_name": "METHYLCELLULOSE (4000 MPA.S)",
    "substance_type": "polymer",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9d5f2244-a610-4d45-b6e8-e79bb17a558f": {
      "match": "brand_token",
      "title": "CITRUCEL (METHYLCELLULOSE) POWDER, FOR SOLUTION [HALEON US HOLDINGS LLC]",
      "spl_version": "17",
      "published_date": "2026-03-20"
    }
  },
  "productid": "0135-0199_6df5275a-78c1-452c-a061-4202a131969f",
  "productndc": "0135-0199",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "METHYLCELLULOSE (4000 MPA.S)",
  "proprietary_name": "CITRUCEL",
  "active_ingred_unit": "mg/1",
  "application_number": "M007",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "methylcellulose",
  "start_marketing_date": "20100201",
  "active_numerator_strength": "500"
}

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