Smart Care SEA BREEZE HAND SANITIZER

Product NDC
70108-299
11-digit product format
701080299
Labeler code
70108
Product ID
70108-299_174b191c-5cae-4d0f-957f-a80ec9977364
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
2026-01-15
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Smart Care SEA BREEZE HAND SANITIZER
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL70 mL/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M
Rxcui1041849

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70108-299-01Smart Care SEA BREEZE HAND SANITIZER1 in 1 POUCHSPRAY11
70108-299-01Smart Care SEA BREEZE HAND SANITIZER40 mL in 1 BOTTLE, SPRAYSPRAY401

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1041849ethanol 70 % Topical SprayPSNd98cddef-e846-4e6f-939b-d854221399f71
1041849ethanol 0.7 ML/ML Topical SpraySCDd98cddef-e846-4e6f-939b-d854221399f71
1041849ethanol 70 % Topical SpraySYd98cddef-e846-4e6f-939b-d854221399f71

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
70108-299-01701080299011 BOTTLE, SPRAY in 1 POUCH (70108-299-01) / 40 mL in 1 BOTTLE, SPRAY2026-01-15NoNoCurrent