rugby anti-dandruff
Generic: selenium sulfide
Labeler: rugby laboratoriesDrug Facts
Product Profile
Brand Name
rugby anti-dandruff
Generic Name
selenium sulfide
Labeler
rugby laboratories
Dosage Form
SHAMPOO
Routes
Active Ingredients
selenium sulfide 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0536-1995
Product ID
0536-1995_50c4b8c0-9787-407e-9fa6-d6a03ea4323e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2026-12-31
Marketing Start
2012-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05361995
Hyphenated Format
0536-1995
Supplemental Identifiers
RxCUI
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
rugby anti-dandruff (source: ndc)
Generic Name
selenium sulfide (source: ndc)
Application Number
M032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 207 mL in 1 BOTTLE, PLASTIC (0536-1995-53)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "50c4b8c0-9787-407e-9fa6-d6a03ea4323e", "openfda": {"unii": ["Z69D9E381Q"], "rxcui": ["204642"], "spl_set_id": ["f8942f2b-32fb-4a2d-b0cf-0f2d1c6974c2"], "manufacturer_name": ["Rugby Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "207 mL in 1 BOTTLE, PLASTIC (0536-1995-53)", "package_ndc": "0536-1995-53", "marketing_start_date": "20120501"}], "brand_name": "Rugby Anti-Dandruff", "product_id": "0536-1995_50c4b8c0-9787-407e-9fa6-d6a03ea4323e", "dosage_form": "SHAMPOO", "product_ndc": "0536-1995", "generic_name": "Selenium Sulfide", "labeler_name": "Rugby Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rugby Anti-Dandruff", "active_ingredients": [{"name": "SELENIUM SULFIDE", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120501", "listing_expiration_date": "20261231"}