# Lil Drug Store Pain Relief All Day

NDC: 66715-9740
Generic name: Naproxen Sodium
Labeler / Manufacturer: Lil' Drug Store Products, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20110127
Marketing ended: 20270102
FDA application: ANDA079096

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66715-9740"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66715-9740
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=41d2d995-47ef-419d-8e57-ea3f9f8a9f68