dzul anti-dandruff
Generic: zinc pyrithione
Labeler: caball sales, inc.Drug Facts
Product Profile
Brand Name
dzul anti-dandruff
Generic Name
zinc pyrithione
Labeler
caball sales, inc.
Dosage Form
SHAMPOO
Routes
Active Ingredients
pyrithione zinc 1 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
83037-001
Product ID
83037-001_47e60c2d-c9aa-e9c4-e063-6294a90afe19
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2027-12-31
Marketing Start
2023-09-22
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83037001
Hyphenated Format
83037-001
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
dzul anti-dandruff (source: ndc)
Generic Name
zinc pyrithione (source: ndc)
Application Number
M032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/100mL
Packaging
- 236 mL in 1 BOTTLE (83037-001-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "47e60c2d-c9aa-e9c4-e063-6294a90afe19", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["05e3fac4-c0ce-cbb9-e063-6294a90ac036"], "manufacturer_name": ["Caball Sales, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 BOTTLE (83037-001-08)", "package_ndc": "83037-001-08", "marketing_start_date": "20230922"}], "brand_name": "DZUL ANTI-DANDRUFF", "product_id": "83037-001_47e60c2d-c9aa-e9c4-e063-6294a90afe19", "dosage_form": "SHAMPOO", "product_ndc": "83037-001", "generic_name": "Zinc Pyrithione", "labeler_name": "Caball Sales, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DZUL ANTI-DANDRUFF", "active_ingredients": [{"name": "PYRITHIONE ZINC", "strength": "1 g/100mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230922", "listing_expiration_date": "20271231"}