Degree

Product NDC
64942-2281
11-digit product format
649422281
Labeler code
64942
Product ID
64942-2281_18fdfebe-75b9-3b45-e063-6394a90a9aba
Type
HUMAN OTC DRUG
Nonproprietary name
Advanced Extreme Blast 72H Antiperspirant Deodorant
Dosage form
STICK
Route
TOPICAL
Labeler
Conopco Inc. d/b/a/ Unilever
Application
M019
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-07-01
Substance
ALUMINUM SESQUICHLOROHYDRATE
Active strength
16 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA Listing Details

Product ID
64942-2281_18fdfebe-75b9-3b45-e063-6394a90a9aba
SPL ID
18fdfebe-75b9-3b45-e063-6394a90a9aba
Product type
HUMAN OTC DRUG
Finished product
Yes
Brand name base
Degree
Generic name
Advanced Extreme Blast 72H Antiperspirant Deodorant
Dosage form
STICK
Route
TOPICAL
Marketing start
2024-07-01
Marketing category
OTC MONOGRAPH DRUG
Application number
M019
Listing expiration
2026-12-31

openFDA Active Ingredients

IngredientStrength
ALUMINUM SESQUICHLOROHYDRATE16 g/100g

openFDA Harmonized Identifiers

FieldValues
UniiUCN889409V
Spl Set Id18fdf749-5c74-7c5f-e063-6294a90a9cdc
Manufacturer NameConopco Inc. d/b/a/ Unilever

openFDA Package Details

Package NDCDescriptionMarketing startSample
64942-2281-176 g in 1 CONTAINER (64942-2281-1)2024-07-01No
64942-2281-22 CONTAINER in 1 CONTAINER (64942-2281-2) / 76 g in 1 CONTAINER (64942-2281-1)2024-07-01No

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
UCN889409VALUMINUM SESQUICHLOROHYDRATE1327-41-9ALUMINUM SESQUICHLOROHYDRATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
64942-2281-16494222810176 g in 1 CONTAINER (64942-2281-1) 76 g2024-07-01NoNoHistorical
64942-2281-2649422281022 CONTAINER in 1 CONTAINER (64942-2281-2) / 76 g in 1 CONTAINER (64942-2281-1) 2 container2024-07-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Degree Advanced Extreme Blast 72H Antiperspirant DeodorantConopco Inc. d/b/a/ Unilever2024-05-21HUMAN OTC DRUG LABEL1