Package 12022-007-00

Brand: glovers dandruff control medicine, regular

Generic: sulfur
NDC Package

Package Facts

Identity

Package NDC 12022-007-00
Digits Only 1202200700
Product NDC 12022-007
Product ID 12022-007_08340897-23b3-f23b-e063-6294a90a4eb9
Description

1 BOTTLE in 1 CARTON (12022-007-00) / 81 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2001-09-24
Brand glovers dandruff control medicine, regular
Generic sulfur
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": "08340897-23b3-f23b-e063-6294a90a4eb9", "openfda": {"upc": ["0310471011437"], "unii": ["70FD1KFU70"], "rxcui": ["247683"], "spl_set_id": ["18700036-11ec-4370-bcc6-b9e2c732e7d9"], "manufacturer_name": ["J. Strickland & Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (12022-007-00)  / 81 mL in 1 BOTTLE", "package_ndc": "12022-007-00", "marketing_start_date": "20010924"}], "brand_name": "Glovers Dandruff Control Medicine, Regular", "product_id": "12022-007_08340897-23b3-f23b-e063-6294a90a4eb9", "dosage_form": "SUSPENSION", "product_ndc": "12022-007", "generic_name": "Sulfur", "labeler_name": "J. Strickland & Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Glovers Dandruff Control Medicine, Regular", "active_ingredients": [{"name": "SULFUR", "strength": "25 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20010924", "listing_expiration_date": "20261231"}