Home NDC 59779-070 Advanced Hand Sanitizer
Product NDC 59779-070
11-digit product format 597790070
Labeler code 59779
Product ID 59779-070_49ecdd80-27ef-fead-e063-6394a90a7787
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler CVS Pharmacy, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-10-18
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59779-070-49 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59779-070-45 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59779-070-26 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59779-070-49 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59779-070-45 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59779-070-26 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 59779-070-15 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 59779-070-15 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 59779-070-15 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 59779-070-15 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…
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 Advanced Hand Sanitizer
Listing expiration 2027-12-31 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 581662 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59779-070-16 Advanced Hand Sanitizer 59 mL in 1 BOTTLE, DISPENSING GEL 59 26 59779-070-26 Advanced Hand Sanitizer 118 mL in 1 BOTTLE, DISPENSING GEL 118 26 59779-070-34 Advanced Hand Sanitizer 236 mL in 1 BOTTLE, PUMP GEL 236 26 59779-070-45 Advanced Hand Sanitizer 946 mL in 1 BOTTLE, PLASTIC GEL 946 26 59779-070-49 Advanced Hand Sanitizer 443 mL in 1 BOTTLE, PUMP GEL 443 26
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALCOHOL ACTIVE INGREDIENT 3K9958V90M ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 ALCOHOL ACTIVE MOIETY 3K9958V90M ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) INACTIVE INGREDIENT 59TL3WG5CO ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 FD&C YELLOW NO. 5 INACTIVE INGREDIENT I753WB2F1M ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 GLYCERYL CAPRYLATE/CAPRATE INACTIVE INGREDIENT G7515SW10N ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 SULISOBENZONE INACTIVE INGREDIENT 1W6L629B4K ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2 WATER INACTIVE INGREDIENT 059QF0KO0R ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59779-070 ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [CVS PHARMACY, INC] 24 Current NDC, Legacy NDC, 5 package rows 20240808_2adb16b7-c43f-49a0-9a56-fece3d730089.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 Units Marketing start Marketing end Sample Exclude flag Status 59779-070-16 59779007016 59 mL in 1 BOTTLE, DISPENSING (59779-070-16) 59 ml 2013-10-18 0000-00-00 No No Current 59779-070-26 59779007026 118 mL in 1 BOTTLE, DISPENSING (59779-070-26) 118 ml 2013-10-18 0000-00-00 No No Current 59779-070-34 59779007034 236 mL in 1 BOTTLE, PUMP (59779-070-34) 236 ml 2013-10-18 0000-00-00 No No Current 59779-070-45 59779007045 946 mL in 1 BOTTLE, PLASTIC (59779-070-45) 946 ml 2013-10-18 0000-00-00 No No Current 59779-070-49 59779007049 443 mL in 1 BOTTLE, PUMP (59779-070-49) 443 ml 2013-10-18 0000-00-00 No No Current