# Nicorette White Ice Mint

NDC: 0135-0474
Generic name: nicotine polacrilex
Labeler / Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GUM, CHEWING
Routes: ORAL
Marketing started: 20090629

FDA application: NDA018612

## Active ingredients

- NICOTINE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0135-0474"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0135-0474
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=673fd19f-69b3-4f73-b9b4-18b5f4cbf69c