dandruff
Generic: selenium sulfide
Labeler: h e bDrug Facts
Product Profile
Brand Name
dandruff
Generic Name
selenium sulfide
Labeler
h e b
Dosage Form
SHAMPOO
Routes
Active Ingredients
selenium sulfide 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
37808-816
Product ID
37808-816_4b9417c3-3492-abab-e063-6294a90a9ac3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2027-12-31
Marketing Start
2016-09-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808816
Hyphenated Format
37808-816
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dandruff (source: ndc)
Generic Name
selenium sulfide (source: ndc)
Application Number
M032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 420 mL in 1 BOTTLE, PLASTIC (37808-816-15)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}