Home NDC 59735-160 Your Name Cosmetics Brightening CC Cream Broad Spectrum SPF 20
Product NDC 59735-160
11-digit product format 597350160
Labeler code 59735
Product ID 59735-160_491f8925-b1e8-3372-e054-00144ff8d46c
Type HUMAN OTC DRUG
Nonproprietary name Your Name Cosmetics Brightening CC Cream Broad Spectrum SPF 20
Dosage form LOTION
Route TOPICAL
Labeler Mana Products
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2017-02-21
Substance OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 7.5; 5; .99 g/100g; g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Your Name Cosmetics Brightening CC Cream Broad Spectrum SPF 20
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7.5 g/100g TITANIUM DIOXIDE 5 g/100g ZINC OXIDE .99 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4Y5P7MUD51 Internal UNII lookup 15FIX9V2JP Internal UNII lookup SOI2LOH54Z 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 59735-160-01 Your Name Cosmetics Brightening CC Cream Broad Spectrum SPF 20 33 g in 1 TUBE LOTION 33 1 59735-160-01 Your Name Cosmetics Brightening CC Cream Broad Spectrum SPF 20 1 in 1 CARTON LOTION 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59735-160 YOUR NAME COSMETICS BRIGHTENING CC CREAM BROAD SPECTRUM SPF 20 LOTION [MANA PRODUCTS] 1 Current NDC, Legacy NDC, 2 package rows 20170222_ae6a86d2-a95b-4fa8-9676-233ef9fdc3b0.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 1 of 1 · 1 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 59735-160-01 59735016001 1 TUBE in 1 CARTON (59735-160-01) / 33 g in 1 TUBE 1 tube 2017-02-21 0000-00-00 No No Current