Home NDC 84509-034 Sulfur anti-mite shower gel
Product NDC 84509-034
11-digit product format 845090034
Labeler code 84509
Product ID 84509-034_2b3ee9e5-938d-a1dd-e063-6294a90a59c6
Type HUMAN OTC DRUG
Nonproprietary name Sodium Laureth Sulfat,Decyl Glucoside,Palm Kernelamide DEA,Cocamidopropyl Betaine,Lonicera Japonica(Honeysuckle) Flower Extract,Colloidal Sulfur.
Dosage form LIQUID
Route TOPICAL
Labeler Guangdong Junhui Biotechnology Co., Ltd
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-10-23
Substance SODIUM; LONICERA JAPONICA FLOWER; DECYL GLUCOSIDE; COCAMIDOPROPYL BETAINE; PALM KERNEL OIL; SULFUR
Active strength 25200; 10500; 5100; 3000; 3000; 600 mg/300mL; mg/300mL; mg/300mL; mg/300mL; mg/300mL; mg/300mL
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 Sulfur anti-mite shower gel
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM 25200 mg/300mL LONICERA JAPONICA FLOWER 10500 mg/300mL DECYL GLUCOSIDE 5100 mg/300mL COCAMIDOPROPYL BETAINE 3000 mg/300mL PALM KERNEL OIL 3000 mg/300mL SULFUR 600 mg/300mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 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 84509-034-01 Sulfur anti-mite shower gel 300 mL in 1 BOTTLE LIQUID 300 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84509-034 SULFUR ANTI-MITE SHOWER GEL (SODIUM LAURETH SULFAT,DECYL GLUCOSIDE,PALM KERNELAMIDE DEA,COCAMIDOPROPYL BETAINE,LONICERA JAPONICA(HONEYSUCKLE) FLOWER EXTRACT,COLLOIDAL SULFUR.) LIQUID [GUANGDONG JUNHUI BIOTECHNOLOGY CO., LTD] 2 Current NDC, 1 package rows 20250110_251ee057-1adf-bc97-e063-6394a90acdd3.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 39 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84509-034-01 84509003401 300 mL in 1 BOTTLE (84509-034-01) 300 ml 2024-10-23 No No Current