kiehls since 1851 ultra facial moisturizer broad spectrum spf 30 sunscreen for all skin types

Generic: avobenzone, homosalate, octisalate and octocrylene

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 ultra facial moisturizer broad spectrum spf 30 sunscreen for all skin types
Generic Name avobenzone, homosalate, octisalate and octocrylene
Labeler l'oreal usa products inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 70 mg/mL, octisalate 50 mg/mL, octocrylene 50 mg/mL

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-797
Product ID 49967-797_e96dab17-d26d-4fb5-9e40-b88d0bdcbf7a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2013-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49967797
Hyphenated Format 49967-797

Supplemental Identifiers

UPC
3605970387976
UNII
G63QQF2NOX V06SV4M95S 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 kiehls since 1851 ultra facial moisturizer broad spectrum spf 30 sunscreen for all skin types (source: ndc)
Generic Name avobenzone, homosalate, octisalate and octocrylene (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
  • 70 mg/mL
  • 50 mg/mL
source: ndc
Packaging
  • 250 mL in 1 BOTTLE (49967-797-01)
  • 125 mL in 1 BOTTLE (49967-797-02)
  • 75 mL in 1 BOTTLE (49967-797-03)
  • 30 mL in 1 BOTTLE (49967-797-04)
  • 3 mL in 1 PACKET (49967-797-05)
source: ndc

Packages (5)

49967-797-01 250 mL in 1 BOTTLE (49967-797-01) 49967-797-02 125 mL in 1 BOTTLE (49967-797-02) 49967-797-03 75 mL in 1 BOTTLE (49967-797-03) 49967-797-04 30 mL in 1 BOTTLE (49967-797-04) 49967-797-05 3 mL in 1 PACKET (49967-797-05)

Ingredients (4)

avobenzone (30 mg/mL) homosalate (70 mg/mL) octisalate (50 mg/mL) octocrylene (50 mg/mL)

Linked Drug Pages (1)

Kiehls Since 1851 Ultra Facial Moisturizer Broad Spectrum SPF 30 Sunscreen For All Skin Types ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "e96dab17-d26d-4fb5-9e40-b88d0bdcbf7a", "openfda": {"upc": ["3605970387976"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["d1a8c8d2-59d2-4389-9369-5f9b053a956e"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BOTTLE (49967-797-01)", "package_ndc": "49967-797-01", "marketing_start_date": "20130301"}, {"sample": false, "description": "125 mL in 1 BOTTLE (49967-797-02)", "package_ndc": "49967-797-02", "marketing_start_date": "20130301"}, {"sample": false, "description": "75 mL in 1 BOTTLE (49967-797-03)", "package_ndc": "49967-797-03", "marketing_start_date": "20130301"}, {"sample": false, "description": "30 mL in 1 BOTTLE (49967-797-04)", "package_ndc": "49967-797-04", "marketing_start_date": "20130301"}, {"sample": false, "description": "3 mL in 1 PACKET (49967-797-05)", "package_ndc": "49967-797-05", "marketing_start_date": "20130301"}], "brand_name": "Kiehls Since 1851 Ultra Facial Moisturizer Broad Spectrum SPF 30 Sunscreen For All Skin Types", "product_id": "49967-797_e96dab17-d26d-4fb5-9e40-b88d0bdcbf7a", "dosage_form": "LOTION", "product_ndc": "49967-797", "generic_name": "Avobenzone, Homosalate, Octisalate and Octocrylene", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kiehls Since 1851 Ultra Facial Moisturizer Broad Spectrum SPF 30 Sunscreen For All Skin Types", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "70 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "50 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}