Home NDC 11673-934 Up and Up
Product NDC 11673-934
11-digit product format 116730934
Labeler code 11673
Product ID 11673-934_2476623c-2e31-7a6b-e063-6294a90aea58
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Octinoxate, Octisalate
Dosage form LOTION
Route TOPICAL
Labeler TARGET CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-02-01
Substance OCTISALATE; OCTINOXATE; AVOBENZONE
Active strength 20; 75; 30 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 Up and Up
Brand name suffix Illuminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 20 mg/mL OCTINOXATE 75 mg/mL AVOBENZONE 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup G63QQF2NOX Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-934-04 Up and UpIlluminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15 118.3 mL in 1 BOTTLE LOTION 118.3 3 11673-934-05 Up and UpIlluminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15 1 in 1 CARTON LOTION 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-934 UP AND UP ILLUMINATING DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 15 (AVOBENZONE, OCTINOXATE, OCTISALATE) LOTION [TARGET CORPORATION] 3 Current NDC, Legacy NDC, 2 package rows 20241016_9407a4a9-8a72-6a01-e053-2a95a90a231d.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 Units Marketing start Marketing end Sample Exclude flag Status 11673-934-04 11673093404 118.3 mL in 1 BOTTLE 118.3 ml Historical 11673-934-05 11673093405 1 BOTTLE in 1 CARTON (11673-934-05) / 118.3 mL in 1 BOTTLE (11673-934-04) 1 bottle 2013-02-01 0000-00-00 No No Current