Home NDC 79265-8072 Babo Botanicals SPF 30 Daily Sheer Tinted Sunscreen - Natural Glow
Product NDC 79265-8072
11-digit product format 792658072
Labeler code 79265
Product ID 79265-8072_2915d6ea-54aa-f2bf-e063-6294a90a22ba
Type HUMAN OTC DRUG
Nonproprietary name Mineral Sunscreen
Dosage form LOTION
Route TOPICAL
Labeler Babo Botanicals, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-07-24
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 3000; 3000 mg/100mL; mg/100mL
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 Babo Botanicals SPF 30 Daily Sheer Tinted Sunscreen - Natural Glow
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 3000 mg/100mL ZINC OXIDE 3000 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII lookup
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 79265-8072-0 Babo Botanicals SPF 30 Daily Sheer Tinted Sunscreen - Natural Glow 1 in 1 BOX LOTION 1 7 79265-8072-1 Babo Botanicals SPF 30 Daily Sheer Tinted Sunscreen - Natural Glow 50 mL in 1 TUBE LOTION 50 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79265-8072 BABO BOTANICALS SPF 30 DAILY SHEER TINTED SUNSCREEN - NATURAL GLOW (MINERAL SUNSCREEN) LOTION [BABO BOTANICALS, INC.] 7 Current NDC, Legacy NDC, 2 package rows 20241215_ab39d9f0-d869-6f33-e053-2995a90a08d4.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 353 · 7,049 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 79265-8072-0 79265807200 1 TUBE in 1 BOX (79265-8072-0) / 50 mL in 1 TUBE (79265-8072-1) 1 tube 2020-07-24 0000-00-00 No No Current 79265-8072-1 79265807201 50 mL in 1 TUBE 50 ml Historical