Package 42192-135-10

Brand: salicylic acid

Generic: salicylic acid
NDC Package

Package Facts

Identity

Package NDC 42192-135-10
Digits Only 4219213510
Product NDC 42192-135
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (42192-135-10) / 10 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2011-10-10
Brand salicylic acid
Generic salicylic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "56e0544c-2352-4ee3-8a07-2936853ae97f", "openfda": {"unii": ["O414PZ4LPZ"], "rxcui": ["1095689"], "spl_set_id": ["572171f7-832f-4710-b888-eef5638fc9d4"], "manufacturer_name": ["Acella Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (42192-135-10)  / 10 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "42192-135-10", "marketing_start_date": "20111010"}], "brand_name": "SALICYLIC ACID", "product_id": "42192-135_56e0544c-2352-4ee3-8a07-2936853ae97f", "dosage_form": "LIQUID", "product_ndc": "42192-135", "generic_name": "SALICYLIC ACID", "labeler_name": "Acella Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SALICYLIC ACID", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "275 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20111010", "listing_expiration_date": "20261231"}