lebelage uv sun ultra shield sun screenlotion 50g

Generic: avobenzone, homosalate, octinoxate, octocrylene, octisalate

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

Drug Facts

Product Profile

Brand Name lebelage uv sun ultra shield sun screenlotion 50g
Generic Name avobenzone, homosalate, octinoxate, octocrylene, octisalate
Labeler dongdonggurimoo co.,ltd.
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 1.5 g/50g, homosalate 5 g/50g, octinoxate 3.5 g/50g, octisalate 2.5 g/50g, octocrylene 5 g/50g

Manufacturer
DONGDONGGURIMOO CO.,LTD.

Identifiers & Regulatory

Product NDC 85948-251
Product ID 85948-251_4907e7bc-0f93-3d89-e063-6394a90aedde
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2027-12-31
Marketing Start 2026-01-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 85948251
Hyphenated Format 85948-251

Supplemental Identifiers

UNII
G63QQF2NOX V06SV4M95S 4Y5P7MUD51 4X49Y0596W 5A68WGF6WM

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 lebelage uv sun ultra shield sun screenlotion 50g (source: ndc)
Generic Name avobenzone, homosalate, octinoxate, octocrylene, octisalate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/50g
  • 5 g/50g
  • 3.5 g/50g
  • 2.5 g/50g
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (85948-251-02) / 50 g in 1 BOTTLE, PLASTIC (85948-251-01)
source: ndc

Packages (1)

85948-251-02 1 BOTTLE, PLASTIC in 1 BOX (85948-251-02) / 50 g in 1 BOTTLE, PLASTIC (85948-251-01)

Ingredients (5)

avobenzone (1.5 g/50g) homosalate (5 g/50g) octinoxate (3.5 g/50g) octisalate (2.5 g/50g) octocrylene (5 g/50g)

Linked Drug Pages (1)

LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4907e7bc-0f93-3d89-e063-6394a90aedde", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4Y5P7MUD51", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["4907eb9c-3978-27ed-e063-6394a90a9f66"], "manufacturer_name": ["DONGDONGGURIMOO CO.,LTD."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (85948-251-02)  / 50 g in 1 BOTTLE, PLASTIC (85948-251-01)", "package_ndc": "85948-251-02", "marketing_start_date": "20260112"}], "brand_name": "LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g", "product_id": "85948-251_4907e7bc-0f93-3d89-e063-6394a90aedde", "dosage_form": "LOTION", "product_ndc": "85948-251", "generic_name": "AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE, OCTISALATE", "labeler_name": "DONGDONGGURIMOO CO.,LTD.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g", "active_ingredients": [{"name": "AVOBENZONE", "strength": "1.5 g/50g"}, {"name": "HOMOSALATE", "strength": "5 g/50g"}, {"name": "OCTINOXATE", "strength": "3.5 g/50g"}, {"name": "OCTISALATE", "strength": "2.5 g/50g"}, {"name": "OCTOCRYLENE", "strength": "5 g/50g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260112", "listing_expiration_date": "20271231"}