Package 58414-0017-2

Brand: exuviance daily acne peel

Generic: salicylic acid
NDC Package

Package Facts

Identity

Package NDC 58414-0017-2
Digits Only 5841400172
Product NDC 58414-0017
Product ID 58414-0017_2b593fd9-8310-5dc4-e063-6394a90ad6f3
Description

1 BOTTLE, PLASTIC in 1 CARTON (58414-0017-2) / 100 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2019-12-01
Brand exuviance daily acne peel
Generic salicylic acid
Sample Package No

Linked Drug Pages (1)

Exuviance Daily Acne Peel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2b593fd9-8310-5dc4-e063-6394a90ad6f3", "openfda": {"upc": ["0732013203344"], "unii": ["O414PZ4LPZ"], "rxcui": ["251577"], "spl_set_id": ["e9f7da8a-c595-4500-89f1-ec8a2a72ef59"], "manufacturer_name": ["NeoStrata Company Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (58414-0017-2)  / 100 mL in 1 BOTTLE, PLASTIC", "package_ndc": "58414-0017-2", "marketing_start_date": "20191201"}], "brand_name": "Exuviance Daily Acne Peel", "product_id": "58414-0017_2b593fd9-8310-5dc4-e063-6394a90ad6f3", "dosage_form": "LIQUID", "product_ndc": "58414-0017", "generic_name": "SALICYLIC ACID", "labeler_name": "NeoStrata Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Exuviance Daily Acne Peel", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "20 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180615", "listing_expiration_date": "20261231"}