Moxie

Product NDC
63148-660
11-digit product format
631480660
Labeler code
63148
Product ID
63148-660_51177faa-2411-fc43-e063-6294a90ab0c7
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
Apollo Health and Beauty Care
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-03-02
Substance
ALCOHOL
Active strength
700 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Moxie
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL700 mg/mL

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
581662Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
3752d034-d4b4-47ab-b1bb-066cef7fde75Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63148-660-24Moxie710 mL in 1 BOTTLE, PLASTICGEL7104
63148-660-50Moxie1470 mL in 1 BOTTLE, PLASTICGEL14704

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63148-660MOXIE (ETHYL ALCOHOL) GEL [APOLLO HEALTH AND BEAUTY CARE]2Current NDC, Legacy NDC, 2 package rows20250106_3752d034-d4b4-47ab-b1bb-066cef7fde75.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
MoxieETHYL ALCOHOLApollo Health and Beauty Care3752d034-d4b4-47ab-b1bb-066cef7fde752026-05-05WarningsExact identifier
ndc (product): 63148-660

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSN3752d034-d4b4-47ab-b1bb-066cef7fde754
581662ethanol 0.7 ML/ML Topical GelSCD3752d034-d4b4-47ab-b1bb-066cef7fde754
581662ethanol 70 % Topical GelSY3752d034-d4b4-47ab-b1bb-066cef7fde754
581662ethyl alcohol 70 % Topical GelSY3752d034-d4b4-47ab-b1bb-066cef7fde754

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63148-660-2463148066024710 mL in 1 BOTTLE, PLASTIC (63148-660-24) 710 ml2021-03-020000-00-00NoNoCurrent
63148-660-50631480660501470 mL in 1 BOTTLE, PLASTIC (63148-660-50) 1470 ml2021-03-020000-00-00NoNoCurrent