Home NDC 69423-259 Olay Age Defying Classic Daily Renewal
Product NDC 69423-259
11-digit product format 694230259
Labeler code 69423
Product ID 69423-259_47458671-a500-98da-e063-6394a90a69e3
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate and Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler The Procter & Gamble Manufacturing Company
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-08-11
Substance OCTINOXATE; ZINC OXIDE
Active strength 6; 3 g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 69423-259-12 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 69423-259-12 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 69423-259-12 bd6a592717d7…303034d00443…
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 Olay Age Defying Classic Daily Renewal
Brand name suffix Broad Spectrum SPF 15
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 6 g/100mL ZINC OXIDE 3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69423-259-12 Olay Age Defying Classic Daily RenewalBroad Spectrum SPF 15 1 in 1 CARTON LOTION 1 5 69423-259-12 Olay Age Defying Classic Daily RenewalBroad Spectrum SPF 15 120 mL in 1 BOTTLE, PLASTIC LOTION 120 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-259 OLAY AGE DEFYING CLASSIC DAILY RENEWAL BROAD SPECTRUM SPF 15 (OCTINOXATE AND ZINC OXIDE) LOTION [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 4 Current NDC, Legacy NDC, 2 package rows 20240927_60183a47-fd02-052b-e053-2991aa0a1b5c.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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69423-259-12 69423025912 1 BOTTLE, PLASTIC in 1 CARTON (69423-259-12) / 120 mL in 1 BOTTLE, PLASTIC 2017-08-11 0000-00-00 No No Current