Home NDC 49967-099 Kiehls Since 1851 Ultra Facial Broad Spectrum SPF 30 Sunscreen
Product NDC 49967-099
11-digit product format 499670099
Labeler code 49967
Product ID 49967-099_a53bdd11-49ff-4178-a9da-290ed588308e
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate and Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler L�Oreal USA Products Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-11-01
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 50; 50; 70 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Kiehls Since 1851 Ultra Facial Broad Spectrum SPF 30 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 50 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 70 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49967-099-01 Kiehls Since 1851 Ultra Facial Broad Spectrum SPF 30 Sunscreen 50 mL in 1 JAR CREAM 50 6 49967-099-02 Kiehls Since 1851 Ultra Facial Broad Spectrum SPF 30 Sunscreen 125 mL in 1 JAR CREAM 125 6 49967-099-03 Kiehls Since 1851 Ultra Facial Broad Spectrum SPF 30 Sunscreen 3 mL in 1 PACKET CREAM 3 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-099 KIEHLS SINCE 1851 ULTRA FACIAL BROAD SPECTRUM SPF 30 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE) CREAM [L’OREAL USA PRODUCTS INC] 6 Current NDC, Legacy NDC, 3 package rows 20231231_fb9daea3-c249-417c-ad34-3e89f3118559.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 81 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49967-099-01 49967009901 50 mL in 1 JAR (49967-099-01) 50 ml 2015-11-01 0000-00-00 No No Current 49967-099-02 49967009902 125 mL in 1 JAR (49967-099-02) 125 ml 2015-11-01 0000-00-00 No No Current 49967-099-03 49967009903 3 mL in 1 PACKET (49967-099-03) 3 ml 2015-11-01 0000-00-00 No No Current