Home NDC 71714-008 Tiege Hanley AM Morning Facial Moisturizer with SPF 20
Product NDC 71714-008
11-digit product format 717140008
Labeler code 71714
Product ID 71714-008_5d30a56b-152d-5598-e063-6294a90a9bd1
Type HUMAN OTC DRUG
Nonproprietary name Avobenzene, homosalate, octisalate, octocrylene
Dosage form LOTION
Route TOPICAL
Labeler TIEGE HANLEY, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-11
Substance OCTISALATE; OCTOCRYLENE; AVOBENZONE; HOMOSALATE
Active strength 50; 30; 30; 73.4 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Tiege Hanley AM Morning Facial Moisturizer with SPF 20
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 50 mg/mL OCTOCRYLENE 30 mg/mL AVOBENZONE 30 mg/mL HOMOSALATE 73.4 mg/mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71714-008-22 Tiege Hanley AM Morning Facial Moisturizer with SPF 20 22 mL in 1 TUBE LOTION 22 1 71714-008-75 Tiege Hanley AM Morning Facial Moisturizer with SPF 20 75 mL in 1 TUBE LOTION 75 1
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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71714-008-22 71714000822 22 mL in 1 TUBE (71714-008-22) 22 ml 2026-02-11 No No Current 71714-008-75 71714000875 75 mL in 1 TUBE (71714-008-75) 75 ml 2026-02-11 No No Current