Home NDC 85819-771-43 SENSITIVE POCKET SUN
Product NDC 85819-771
Requested package NDC 85819-771-43
11-digit product format 858190771
Labeler code 85819
Product ID 85819-771_37938cce-264a-b486-e063-6394a90a17b4
Type HUMAN OTC DRUG
Nonproprietary name SENSITIVE POCKET SUN
Dosage form STICK
Route PERCUTANEOUS
Labeler Shantou Oushiya Biotechnology Co., Ltd
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-07-15
Substance CYCLOPENTASILOXANE; TALC
Active strength 26.5; 15 mg/1; mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SENSITIVE POCKET SUN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TALC 26.5 mg/1 CYCLOPENTASILOXANE 15 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7SEV7J4R1U Internal UNII lookup 0THT5PCI0R 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 85819-771-43 SENSITIVE POCKET SUN 1 in 1 BOTTLE, UNIT-DOSE STICK 1 2 85819-771-43 SENSITIVE POCKET SUN 5 in 1 BOX STICK 5 2
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 Marketing start Sample Exclude flag Status 85819-771-43 85819077143 5 BOTTLE, UNIT-DOSE in 1 BOX (85819-771-43) / 1 STICK in 1 BOTTLE, UNIT-DOSE 2025-07-15 No No Current