mdp uv bio sunscreen

Generic: zinc oxide, homosalate, octocrylene, octisalate

Labeler: skinidea co., ltd
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mdp uv bio sunscreen
Generic Name zinc oxide, homosalate, octocrylene, octisalate
Labeler skinidea co., ltd
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

homosalate 60 mg/mL, octisalate 45 mg/mL, octocrylene 50 mg/mL, zinc oxide 103.8 mg/mL

Manufacturer
SKINIDEA CO., LTD

Identifiers & Regulatory

Product NDC 72220-003
Product ID 72220-003_30877734-91d7-34c8-e063-6294a90a0e64
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2025-03-01

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72220003
Hyphenated Format 72220-003

Supplemental Identifiers

UNII
V06SV4M95S 4X49Y0596W 5A68WGF6WM 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 mdp uv bio sunscreen (source: ndc)
Generic Name zinc oxide, homosalate, octocrylene, octisalate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/mL
  • 45 mg/mL
  • 50 mg/mL
  • 103.8 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (72220-003-02) / 40 mL in 1 TUBE (72220-003-01)
source: ndc

Packages (1)

72220-003-02 1 TUBE in 1 CARTON (72220-003-02) / 40 mL in 1 TUBE (72220-003-01)

Ingredients (4)

homosalate (60 mg/mL) octisalate (45 mg/mL) octocrylene (50 mg/mL) zinc oxide (103.8 mg/mL)

Linked Drug Pages (1)

MDP UV BIO SUNSCREEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "30877734-91d7-34c8-e063-6294a90a0e64", "openfda": {"unii": ["V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "SOI2LOH54Z"], "spl_set_id": ["3087771e-2ab8-2198-e063-6294a90a37d4"], "manufacturer_name": ["SKINIDEA CO., LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (72220-003-02)  / 40 mL in 1 TUBE (72220-003-01)", "package_ndc": "72220-003-02", "marketing_start_date": "20250301"}], "brand_name": "MDP UV BIO SUNSCREEN", "product_id": "72220-003_30877734-91d7-34c8-e063-6294a90a0e64", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "72220-003", "generic_name": "ZINC OXIDE, HOMOSALATE, OCTOCRYLENE, OCTISALATE", "labeler_name": "SKINIDEA CO., LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MDP UV BIO SUNSCREEN", "active_ingredients": [{"name": "HOMOSALATE", "strength": "60 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "50 mg/mL"}, {"name": "ZINC OXIDE", "strength": "103.8 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250301", "listing_expiration_date": "20261231"}