B-Pure Moisturizing Hand SanitizerSugared Strawberry Scented

Product NDC
80684-207
11-digit product format
806840207
Labeler code
80684
Product ID
80684-207_4e090a4a-b37d-deca-e063-6294a90a3fe7
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Fourstar Group USA, Inc.
Application
505(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-03-12
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
B-Pure Moisturizing Hand SanitizerSugared Strawberry Scented
Listing expiration
2027-12-31

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
15e732fe-5c4b-4f3a-9dd5-a4f7015f7542Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80684-207-01B-Pure Moisturizing Hand SanitizerSugared Strawberry Scented34 mL in 1 BOTTLELIQUID341

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
B-Pure Moisturizing Hand SanitizerSugared Strawberry ScentedALCOHOLFourstar Group USA, Inc.15e732fe-5c4b-4f3a-9dd5-a4f7015f75422026-03-27WarningsExact identifier
ndc (product): 80684-207

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1041849ethanol 70 % Topical SprayPSN15e732fe-5c4b-4f3a-9dd5-a4f7015f75421
1041849ethanol 0.7 ML/ML Topical SpraySCD15e732fe-5c4b-4f3a-9dd5-a4f7015f75421
1041849ethanol 70 % Topical SpraySY15e732fe-5c4b-4f3a-9dd5-a4f7015f75421

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80684-207-018068402070134 mL in 1 BOTTLE (80684-207-01) 34 ml2026-03-12NoNoCurrent