# Pain Reliever

NDC: 59726-113
Generic name: Acetaminophen
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: OTC monograph drug
Dosage form: CHEWABLE GEL
Routes: ORAL
Marketing started: 20260630

FDA application: M013

## Active ingredients

- ACETAMINOPHEN: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59726-113"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-113
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fc841cba-8f4f-407b-97de-0422977515bd
