# Sorbitol-Mannitol

NDC: 0990-7981
Generic name: SORBITOL and MANNITOL
Labeler / Manufacturer: ICU Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: IRRIGANT
Routes: URETHRAL
Marketing started: 20191001

FDA application: NDA018316

## Active ingredients

- MANNITOL: .54 g/100mL
- SORBITOL: 2.7 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0990-7981"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0990-7981
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5b44e248-4b7b-4777-954a-921c7b309944