Home NDC 84753-037-01 XUEYI SKIN CARE SUNSCREEN
Product NDC 84753-037
Requested package NDC 84753-037-01
11-digit product format 847530037
Labeler code 84753
Product ID 84753-037_3f605561-e311-5bdb-e063-6394a90a28a8
Type HUMAN OTC DRUG
Nonproprietary name SUNSCREEN
Dosage form CREAM
Route TOPICAL
Labeler Guangdong Bisutang Biotechnology Co., LTD
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-22
Substance OCTOCRYLENE; METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL; ETHYLHEXYL METHOXYCINNAMATE; 4-METHYLBENZYLIDENE CAMPHOR; PHENYLBENZIMIDAZOLE SULFONIC ACID; HONEY; SACCHAROMYCES LYSATE; HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW)
Active strength 3; .75; 5.9958; 2; 1; .001; .00885; .01 mg/100g; mg/100g; mg/100g; mg/100g; mg/100g; mg/100g; mg/100g; mg/100g
NDC exclude flag No
Listing certified through 2026-12-31
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 XUEYI SKIN CARE SUNSCREEN
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 3 mg/100g METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL .75 mg/100g ETHYLHEXYL METHOXYCINNAMATE 5.9958 mg/100g 4-METHYLBENZYLIDENE CAMPHOR 2 mg/100g PHENYLBENZIMIDAZOLE SULFONIC ACID 1 mg/100g HONEY .001 mg/100g SACCHAROMYCES LYSATE .00885 mg/100g HYDROLYSED MARINE COLLAGEN (ENZYMATIC .01 mg/100g 2000 MW)
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 7 matching rows.
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 84753-037-01 XUEYI SKIN CARE SUNSCREEN 48 g in 1 BOTTLE CREAM 48 1
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 Sample Exclude flag Status 84753-037-01 84753003701 48 g in 1 BOTTLE (84753-037-01) 48 g 2025-09-22 No No Current