Home NDC 70108-125-01 Smart Care GOLDEN GROVE HAND SANITIZER
Product NDC 70108-125
Requested package NDC 70108-125-01
11-digit product format 701080125
Labeler code 70108
Product ID 70108-125_ffac1473-7ac7-4644-868d-0bee7751f7c7
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler Ashtel Studios, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-15
Substance ALCOHOL
Active strength 70 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 Smart Care GOLDEN GROVE HAND SANITIZER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 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 1041849 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 70108-125-01 Smart Care GOLDEN GROVE HAND SANITIZER 1 in 1 POUCH SPRAY 1 1 70108-125-01 Smart Care GOLDEN GROVE HAND SANITIZER 40 mL in 1 BOTTLE, SPRAY SPRAY 40 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70108-125 SMART CARE GOLDEN GROVE HAND SANITIZER (ETHYL ALCOHOL) SPRAY [ASHTEL STUDIOS, INC.] 1 Current NDC, 2 package rows 20250416_c2e2ea25-eeef-4143-9b80-aa05daf1de7d.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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 70108-125-01 70108012501 1 BOTTLE, SPRAY in 1 POUCH (70108-125-01) / 40 mL in 1 BOTTLE, SPRAY 2025-04-15 No No Current