Home NDC 59088-413 Hand Sanitizing with Lavender Oil
Product NDC 59088-413
11-digit product format 590880413
Labeler code 59088
Product ID 59088-413_237334e4-0b89-c4b2-e063-6394a90a5540
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler PureTek Corporation
Application M014
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-06-05
Substance ALCOHOL
Active strength 62 mL/100mL
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 Hand Sanitizing with Lavender Oil
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 62 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 581660 Internal RxNorm 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 59088-413-06 Hand Sanitizing with Lavender Oil 1 in 1 KIT GEL 1 3 59088-413-08 Hand Sanitizing with Lavender Oil 118 mL in 1 BOTTLE GEL 118 3 59088-413-14 Hand Sanitizing with Lavender Oil 1 in 1 KIT GEL 1 3 59088-413-31 Hand Sanitizing with Lavender Oil 500 mL in 1 BOTTLE GEL 500 3 59088-413-36 Hand Sanitizing with Lavender Oil 1 in 1 KIT GEL 1 3 59088-413-39 Hand Sanitizing with Lavender Oil 710 mL in 1 BOTTLE GEL 710 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59088-413 HAND SANITIZING WITH LAVENDER OIL (ALCOHOL) GEL [PURETEK CORPORATION] 3 Current NDC, Legacy NDC, 6 package rows 20241004_a75d25a7-1e23-717f-e053-2a95a90a6d93.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 4 of 7 · 135 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59088-413-06 59088041306 1 BOTTLE in 1 KIT (59088-413-06) / 710 mL in 1 BOTTLE (59088-413-39) 1 bottle 2020-06-05 0000-00-00 No No Current 59088-413-08 59088041308 118 mL in 1 BOTTLE 118 ml Historical 59088-413-14 59088041314 1 in 1 KIT Historical 59088-413-31 59088041331 500 mL in 1 BOTTLE (59088-413-31) 500 ml 2020-06-05 0000-00-00 No No Current 59088-413-36 59088041336 1 KIT in 1 KIT (59088-413-36) / 1 BOTTLE in 1 KIT (59088-413-14) / 118 mL in 1 BOTTLE (59088-413-08) 1 kit 2020-06-05 0000-00-00 No No Current 59088-413-39 59088041339 710 mL in 1 BOTTLE 710 ml Historical