la roche posay anthelios sunscreen spf 60 ultra light

Generic: avobenzone, homosalate, octisalate, octocrylene, oxybenzone

Labeler: l'oreal usa, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name la roche posay anthelios sunscreen spf 60 ultra light
Generic Name avobenzone, homosalate, octisalate, octocrylene, oxybenzone
Labeler l'oreal usa, inc.
Dosage Form SPRAY
Routes
TOPICAL
Active Ingredients

avobenzone 27 mg/g, homosalate 96 mg/g, octisalate 29 mg/g, octocrylene 54 mg/g, oxybenzone 35 mg/g

Manufacturer
L'Oreal USA, Inc.

Identifiers & Regulatory

Product NDC 82046-692
Product ID 82046-692_0d120008-eec4-6e06-e063-6294a90a35b9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2014-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82046692
Hyphenated Format 82046-692

Supplemental Identifiers

UPC
0883140500841
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 roche posay anthelios sunscreen spf 60 ultra light (source: ndc)
Generic Name avobenzone, homosalate, octisalate, octocrylene, oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 27 mg/g
  • 96 mg/g
  • 29 mg/g
  • 54 mg/g
  • 35 mg/g
source: ndc
Packaging
  • 143 g in 1 CAN (82046-692-01)
source: ndc

Packages (1)

82046-692-01 143 g in 1 CAN (82046-692-01)

Ingredients (5)

avobenzone (27 mg/g) homosalate (96 mg/g) octisalate (29 mg/g) octocrylene (54 mg/g) oxybenzone (35 mg/g)

Linked Drug Pages (1)

La Roche Posay Anthelios Sunscreen SPF 60 Ultra light ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0d120008-eec4-6e06-e063-6294a90a35b9", "openfda": {"upc": ["0883140500841"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["dad00eee-92cd-7610-e053-2a95a90a1fac"], "manufacturer_name": ["L'Oreal USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "143 g in 1 CAN (82046-692-01)", "package_ndc": "82046-692-01", "marketing_start_date": "20140101"}], "brand_name": "La Roche Posay Anthelios Sunscreen SPF 60 Ultra light", "product_id": "82046-692_0d120008-eec4-6e06-e063-6294a90a35b9", "dosage_form": "SPRAY", "product_ndc": "82046-692", "generic_name": "AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE", "labeler_name": "L'Oreal USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "La Roche Posay Anthelios Sunscreen SPF 60 Ultra light", "active_ingredients": [{"name": "AVOBENZONE", "strength": "27 mg/g"}, {"name": "HOMOSALATE", "strength": "96 mg/g"}, {"name": "OCTISALATE", "strength": "29 mg/g"}, {"name": "OCTOCRYLENE", "strength": "54 mg/g"}, {"name": "OXYBENZONE", "strength": "35 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}