la bodies eclipse sunscreen spf 50

Generic: avobenzone, homosalate, octisalate, octocrylene, and oxybenzone

Labeler: samson pharmaceutical
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name la bodies eclipse sunscreen spf 50
Generic Name avobenzone, homosalate, octisalate, octocrylene, and oxybenzone
Labeler samson pharmaceutical
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/g, homosalate 150 mg/g, octisalate 50 mg/g, octocrylene 24 mg/g, oxybenzone 60 mg/g

Manufacturer
SAMSON PHARMACEUTICAL

Identifiers & Regulatory

Product NDC 20146-4008
Product ID 20146-4008_d11589cb-2061-4c53-8d81-76ebf8a94a96
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2015-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 201464008
Hyphenated Format 20146-4008

Supplemental Identifiers

UPC
0610466030239
UNII
G63QQF2NOX V06SV4M95S 4X49Y0596W 5A68WGF6WM 95OOS7VE0Y

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 la bodies eclipse sunscreen spf 50 (source: ndc)
Generic Name avobenzone, homosalate, octisalate, octocrylene, and oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/g
  • 150 mg/g
  • 50 mg/g
  • 24 mg/g
  • 60 mg/g
source: ndc
Packaging
  • 28 g in 1 TUBE (20146-4008-1)
  • 85 g in 1 TUBE (20146-4008-2)
source: ndc

Packages (2)

20146-4008-1 28 g in 1 TUBE (20146-4008-1) 20146-4008-2 85 g in 1 TUBE (20146-4008-2)

Ingredients (5)

avobenzone (30 mg/g) homosalate (150 mg/g) octisalate (50 mg/g) octocrylene (24 mg/g) oxybenzone (60 mg/g)

Linked Drug Pages (1)

LA Bodies Eclipse Sunscreen SPF 50 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "d11589cb-2061-4c53-8d81-76ebf8a94a96", "openfda": {"upc": ["0610466030239"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["ce3a5ddc-9d4d-4d63-879c-fc4aef9a0a0a"], "manufacturer_name": ["SAMSON PHARMACEUTICAL"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 g in 1 TUBE (20146-4008-1)", "package_ndc": "20146-4008-1", "marketing_start_date": "20150101"}, {"sample": false, "description": "85 g in 1 TUBE (20146-4008-2)", "package_ndc": "20146-4008-2", "marketing_start_date": "20150101"}], "brand_name": "LA Bodies Eclipse Sunscreen SPF 50", "product_id": "20146-4008_d11589cb-2061-4c53-8d81-76ebf8a94a96", "dosage_form": "LOTION", "product_ndc": "20146-4008", "generic_name": "Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone", "labeler_name": "SAMSON PHARMACEUTICAL", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LA Bodies Eclipse Sunscreen SPF 50", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/g"}, {"name": "HOMOSALATE", "strength": "150 mg/g"}, {"name": "OCTISALATE", "strength": "50 mg/g"}, {"name": "OCTOCRYLENE", "strength": "24 mg/g"}, {"name": "OXYBENZONE", "strength": "60 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150101", "listing_expiration_date": "20261231"}