porescreen spf40

Generic: zinc oxide

Labeler: dermalogica, llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name porescreen spf40
Generic Name zinc oxide
Labeler dermalogica, llc.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

zinc oxide 10 mg/100mL

Manufacturer
Dermalogica, LLC.

Identifiers & Regulatory

Product NDC 68479-291
Product ID 68479-291_67812343-d9bc-43df-88d2-85adf578604e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2022-12-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68479291
Hyphenated Format 68479-291

Supplemental Identifiers

UNII
SOI2LOH54Z

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 porescreen spf40 (source: ndc)
Generic Name zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/100mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (68479-291-02) / 30 mL in 1 TUBE
  • 59 mL in 1 TUBE (68479-291-04)
  • 5 mL in 1 TUBE (68479-291-05)
source: ndc

Packages (3)

68479-291-02 1 TUBE in 1 CARTON (68479-291-02) / 30 mL in 1 TUBE 68479-291-04 59 mL in 1 TUBE (68479-291-04) 68479-291-05 5 mL in 1 TUBE (68479-291-05)

Ingredients (1)

zinc oxide (10 mg/100mL)

Linked Drug Pages (1)

PORESCREEN SPF40 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "67812343-d9bc-43df-88d2-85adf578604e", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["37a7362a-b251-4d3a-a957-65d8f338fa12"], "manufacturer_name": ["Dermalogica, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68479-291-02)  / 30 mL in 1 TUBE", "package_ndc": "68479-291-02", "marketing_start_date": "20221201"}, {"sample": false, "description": "59 mL in 1 TUBE (68479-291-04)", "package_ndc": "68479-291-04", "marketing_start_date": "20221201"}, {"sample": false, "description": "5 mL in 1 TUBE (68479-291-05)", "package_ndc": "68479-291-05", "marketing_start_date": "20221201"}], "brand_name": "PORESCREEN SPF40", "product_id": "68479-291_67812343-d9bc-43df-88d2-85adf578604e", "dosage_form": "LOTION", "product_ndc": "68479-291", "generic_name": "Zinc Oxide", "labeler_name": "Dermalogica, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PORESCREEN SPF40", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "10 mg/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}