# Point Relief Coldspot Pain Relieving

NDC: 51452-007
Generic name: MENTHOL
Labeler / Manufacturer: Fabrication Enterprises Inc
Product type: HUMAN OTC DRUG
Marketing category: OTC monograph drug
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20260626

FDA application: M017

## Active ingredients

- MENTHOL: 125 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51452-007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51452-007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=479fb728-4aeb-42e3-b238-f04255514baa