clarins broad spectrum spf 50 dry touch facial sunscreen

Generic: avobenzone, homosalate, octisalate, octocrylene, oxybenzone

Labeler: laboratoires clarins
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name clarins broad spectrum spf 50 dry touch facial sunscreen
Generic Name avobenzone, homosalate, octisalate, octocrylene, oxybenzone
Labeler laboratoires clarins
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 100 mg/mL, octisalate 50 mg/mL, octocrylene 27 mg/mL, oxybenzone 60 mg/mL

Manufacturer
Laboratoires Clarins

Identifiers & Regulatory

Product NDC 58668-9921
Product ID 58668-9921_0bbf5398-06e7-74fb-e063-6294a90a81c7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2024-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 586689921
Hyphenated Format 58668-9921

Supplemental Identifiers

UPC
3666057246074
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 clarins broad spectrum spf 50 dry touch facial sunscreen (source: ndc)
Generic Name avobenzone, homosalate, octisalate, octocrylene, oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
  • 100 mg/mL
  • 50 mg/mL
  • 27 mg/mL
  • 60 mg/mL
source: ndc
Packaging
  • 50 mL in 1 TUBE (58668-9921-1)
source: ndc

Packages (1)

58668-9921-1 50 mL in 1 TUBE (58668-9921-1)

Ingredients (5)

avobenzone (30 mg/mL) homosalate (100 mg/mL) octisalate (50 mg/mL) octocrylene (27 mg/mL) oxybenzone (60 mg/mL)

Linked Drug Pages (1)

CLARINS BROAD SPECTRUM SPF 50 Dry Touch Facial Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0bbf5398-06e7-74fb-e063-6294a90a81c7", "openfda": {"upc": ["3666057246074"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["5bddb1d6-2493-41bf-8c14-73f103c55aa7"], "manufacturer_name": ["Laboratoires Clarins"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 TUBE (58668-9921-1)", "package_ndc": "58668-9921-1", "marketing_start_date": "20240101"}], "brand_name": "CLARINS BROAD SPECTRUM SPF 50 Dry Touch Facial Sunscreen", "product_id": "58668-9921_0bbf5398-06e7-74fb-e063-6294a90a81c7", "dosage_form": "CREAM", "product_ndc": "58668-9921", "generic_name": "AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE", "labeler_name": "Laboratoires Clarins", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CLARINS BROAD SPECTRUM SPF 50 Dry Touch Facial Sunscreen", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "27 mg/mL"}, {"name": "OXYBENZONE", "strength": "60 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}