kiehls since 1851 activated sun protector broad spectrum spf 50 sunscreen water resistant 80 minutes

Generic: avobenzone, homosalate, octisalate, octocrylene and oxybenzone

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

Drug Facts

Product Profile

Brand Name kiehls since 1851 activated sun protector broad spectrum spf 50 sunscreen water resistant 80 minutes
Generic Name avobenzone, homosalate, octisalate, octocrylene and oxybenzone
Labeler l'oreal usa products inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 107.2 mg/mL, octisalate 32.1 mg/mL, octocrylene 60 mg/mL, oxybenzone 38.6 mg/mL

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-047
Product ID 49967-047_d746b613-5513-42fa-b219-c562f9fbc503
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2015-02-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49967047
Hyphenated Format 49967-047

Supplemental Identifiers

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 kiehls since 1851 activated sun protector broad spectrum spf 50 sunscreen water resistant 80 minutes (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/mL
  • 107.2 mg/mL
  • 32.1 mg/mL
  • 60 mg/mL
  • 38.6 mg/mL
source: ndc
Packaging
  • 150 mL in 1 TUBE (49967-047-01)
source: ndc

Packages (1)

Ingredients (5)

avobenzone (30 mg/mL) homosalate (107.2 mg/mL) octisalate (32.1 mg/mL) octocrylene (60 mg/mL) oxybenzone (38.6 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d746b613-5513-42fa-b219-c562f9fbc503", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["04fd0839-5046-4633-a919-6b7b6bea4f3e"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 TUBE (49967-047-01)", "package_ndc": "49967-047-01", "marketing_start_date": "20150215"}], "brand_name": "Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 50 Sunscreen Water Resistant 80 MInutes", "product_id": "49967-047_d746b613-5513-42fa-b219-c562f9fbc503", "dosage_form": "LOTION", "product_ndc": "49967-047", "generic_name": "Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kiehls Since 1851 Activated Sun Protector Broad Spectrum SPF 50 Sunscreen Water Resistant 80 MInutes", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "107.2 mg/mL"}, {"name": "OCTISALATE", "strength": "32.1 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "60 mg/mL"}, {"name": "OXYBENZONE", "strength": "38.6 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150215", "listing_expiration_date": "20261231"}