Home NDC 73898-011 Hand Sanitizer Santal Blanc
Product NDC 73898-011
11-digit product format 738980011
Labeler code 73898
Product ID 73898-011_4692c807-268f-6477-e063-6394a90aac0a
Type HUMAN OTC DRUG
Nonproprietary name Alcohol solution
Dosage form SOLUTION
Route TOPICAL
Labeler Noshinku
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-01
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings Flammable, keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and consult a doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed, get medical help or contact the Poison Control Center right away.
Additional Listing Data#
Finished product Yes
Brand name base Hand Sanitizer Santal Blanc
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
Harmonized Identifiers# Field, Values table Field Values Unii 3K9958V90M Rxcui 582753
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73898-011-20 Hand Sanitizer Santal Blanc 20 mL in 1 BOTTLE, SPRAY SOLUTION 20 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73898-011-20 73898001120 20 mL in 1 BOTTLE, SPRAY (73898-011-20) 20 ml 2026-01-01 No No Current