dermoscribe seborrheic dermatitis

Generic: sulfur, salicylic acid, hydrocortisone

Labeler: dermoscribe pty ltd
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dermoscribe seborrheic dermatitis
Generic Name sulfur, salicylic acid, hydrocortisone
Labeler dermoscribe pty ltd
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

hydrocortisone 1 g/100g, salicylic acid 3 g/100g, sulfur 3 g/100g

Manufacturer
DERMOSCRIBE PTY LTD

Identifiers & Regulatory

Product NDC 69683-202
Product ID 69683-202_4161aee0-5f36-1739-e063-6294a90a5bdf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M032
Listing Expiration 2026-12-31
Marketing Start 2015-03-23

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69683202
Hyphenated Format 69683-202

Supplemental Identifiers

RxCUI
1738574
UNII
WI4X0X7BPJ O414PZ4LPZ 70FD1KFU70
NUI
N0000175576 N0000175450

Packaging Origin

Original Packager
true

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 dermoscribe seborrheic dermatitis (source: ndc)
Generic Name sulfur, salicylic acid, hydrocortisone (source: ndc)
Application Number M032 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 g/100g
  • 3 g/100g
source: ndc
Packaging
  • 60 g in 1 BOTTLE (69683-202-11)
source: ndc

Packages (1)

69683-202-11 60 g in 1 BOTTLE (69683-202-11)

Ingredients (3)

hydrocortisone (1 g/100g) salicylic acid (3 g/100g) sulfur (3 g/100g)

Linked Drug Pages (1)

DERMOSCRIBE SEBORRHEIC DERMATITIS ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4161aee0-5f36-1739-e063-6294a90a5bdf", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["WI4X0X7BPJ", "O414PZ4LPZ", "70FD1KFU70"], "rxcui": ["1738574"], "spl_set_id": ["2b6bf90b-5d42-4c08-afee-56e13122285e"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["DERMOSCRIBE PTY LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 BOTTLE (69683-202-11)", "package_ndc": "69683-202-11", "marketing_start_date": "20150323"}], "brand_name": "DERMOSCRIBE SEBORRHEIC DERMATITIS", "product_id": "69683-202_4161aee0-5f36-1739-e063-6294a90a5bdf", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "69683-202", "generic_name": "SULFUR, SALICYLIC ACID, HYDROCORTISONE", "labeler_name": "DERMOSCRIBE PTY LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DERMOSCRIBE SEBORRHEIC DERMATITIS", "active_ingredients": [{"name": "HYDROCORTISONE", "strength": "1 g/100g"}, {"name": "SALICYLIC ACID", "strength": "3 g/100g"}, {"name": "SULFUR", "strength": "3 g/100g"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150323", "listing_expiration_date": "20261231"}