FRESH FEELS HAND SANITIZER MIST OCEAN BREEZE SCENT

Product NDC
69933-114
11-digit product format
699330114
Labeler code
69933
Product ID
69933-114_37d86e11-93d9-4c17-b774-407182a66fbe
Type
HUMAN OTC DRUG
Nonproprietary name
ETHYL ALCOHOL
Dosage form
SPRAY
Route
TOPICAL
Labeler
Pearl World Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-10-06
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
FRESH FEELS HAND SANITIZER MIST OCEAN BREEZE SCENT
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL70 mL/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
1041849Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
2d37bdef-2927-4d5c-906d-4f6563524cddAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69933-114-04FRESH FEELS HAND SANITIZER MIST OCEAN BREEZE SCENT40 mL in 1 BOTTLE, SPRAYSPRAY401

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
FRESH FEELS HAND SANITIZER MIST OCEAN BREEZE SCENTETHYL ALCOHOLPearl World Inc.2d37bdef-2927-4d5c-906d-4f6563524cdd2025-10-03WarningsExact identifier
ndc (product): 69933-114

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1041849ethanol 70 % Topical SprayPSN2d37bdef-2927-4d5c-906d-4f6563524cdd1
1041849ethanol 0.7 ML/ML Topical SpraySCD2d37bdef-2927-4d5c-906d-4f6563524cdd1
1041849ethanol 70 % Topical SpraySY2d37bdef-2927-4d5c-906d-4f6563524cdd1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69933-114-046993301140440 mL in 1 BOTTLE, SPRAY (69933-114-04) 40 ml2025-10-06NoNoCurrent