Hand Sanitizer

Product NDC
66715-7172
Requested package NDC
66715-7172-8
11-digit product format
667157172
Labeler code
66715
Product ID
66715-7172_2a92a57b-e670-2cec-e063-6294a90ab058
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
Lil' Drug Store Products, Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-06-01
Substance
ALCOHOL
Active strength
62 mg/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 Sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL62 mg/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
581660Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1bb77439-c2b4-431d-8c3b-e78b5431a18aAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66715-7172-8Hand Sanitizer44 mL in 1 BOTTLE, PLASTICGEL444
66715-7172-8Hand Sanitizer12 in 1 CARTONGEL124

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66715-7172HAND SANITIZER (ALCOHOL) GEL [LIL' DRUG STORE PRODUCTS, INC.]4Current NDC, Legacy NDC, 2 package rows20250101_1bb77439-c2b4-431d-8c3b-e78b5431a18a.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hand SanitizerALCOHOLLil' Drug Store Products, Inc.1bb77439-c2b4-431d-8c3b-e78b5431a18a2024-12-31WarningsExact identifier
ndc (package): 66715-7172-8
ndc (product): 66715-7172
ndc11 (package): 66715717208

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581660ethanol 62 % Topical GelPSN1bb77439-c2b4-431d-8c3b-e78b5431a18a4
581660ethanol 0.62 ML/ML Topical GelSCD1bb77439-c2b4-431d-8c3b-e78b5431a18a4
581660ethanol 62 % Topical GelSY1bb77439-c2b4-431d-8c3b-e78b5431a18a4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
66715-7172-86671571720812 BOTTLE, PLASTIC in 1 CARTON (66715-7172-8) / 44 mL in 1 BOTTLE, PLASTIC2019-06-010000-00-00NoNoCurrent