Package 37808-816-15

Brand: dandruff

Generic: selenium sulfide
NDC Package

Package Facts

Identity

Package NDC 37808-816-15
Digits Only 3780881615
Product NDC 37808-816
Product ID 37808-816_4b9417c3-3492-abab-e063-6294a90a9ac3
Description

420 mL in 1 BOTTLE, PLASTIC (37808-816-15)

Marketing

Marketing Status
Marketed Since 2016-09-25
Brand dandruff
Generic selenium sulfide
Sample Package No

Linked Drug Pages (1)

Dandruff ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4b9417c3-3492-abab-e063-6294a90a9ac3", "openfda": {"upc": ["0041220823116"], "unii": ["Z69D9E381Q"], "rxcui": ["204642"], "spl_set_id": ["182ca790-0713-412a-9111-c0cf40f20d02"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE, PLASTIC (37808-816-15)", "package_ndc": "37808-816-15", "marketing_start_date": "20160925"}], "brand_name": "Dandruff", "product_id": "37808-816_4b9417c3-3492-abab-e063-6294a90a9ac3", "dosage_form": "SHAMPOO", "product_ndc": "37808-816", "generic_name": "Selenium sulfide", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dandruff", "active_ingredients": [{"name": "SELENIUM SULFIDE", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160925", "listing_expiration_date": "20271231"}