Package 12022-032-00

Brand: sulfur 8 scalp therapy medicated dandruff control

Generic: salicylic acid
NDC Package

Package Facts

Identity

Package NDC 12022-032-00
Digits Only 1202203200
Product NDC 12022-032
Product ID 12022-032_0834eb14-2e95-ef47-e063-6294a90ad922
Description

355 mL in 1 BOTTLE (12022-032-00)

Marketing

Marketing Status
Marketed Since 2020-01-01
Brand sulfur 8 scalp therapy medicated dandruff control
Generic salicylic acid
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0834eb14-2e95-ef47-e063-6294a90ad922", "openfda": {"upc": ["0075610510102"], "unii": ["O414PZ4LPZ"], "rxcui": ["1048903"], "spl_set_id": ["961ffab9-4e1b-83f3-e053-2a95a90af5fe"], "manufacturer_name": ["J. Strickland and Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (12022-032-00)", "package_ndc": "12022-032-00", "marketing_start_date": "20200101"}], "brand_name": "Sulfur 8 Scalp Therapy Medicated Dandruff Control", "product_id": "12022-032_0834eb14-2e95-ef47-e063-6294a90ad922", "dosage_form": "SPRAY", "product_ndc": "12022-032", "generic_name": "SALICYLIC ACID", "labeler_name": "J. Strickland and Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulfur 8 Scalp Therapy Medicated Dandruff Control", "active_ingredients": [{"name": "SALICYLIC ACID", "strength": "20 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}