FDA.reportPublic FDA data

Nieva Satin

Manufacturer
Genesis Imports & Exports LLC | Teresa Cecena | Genesis Impoirts & Exports LLC | Beiersdorf Manufacturing mexico SA De CV | Roir SA de CV
Effective date
2017-12-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:45

Label at a glance#

ProductNieva Satin
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminium Chorhydrate

OTC - PURPOSE SECTION

Antiperspirant

DOSAGE & ADMINISTRATION SECTION

Reduse underarm perspiration

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep Out of reach of children

WARNINGS SECTION

Fpr external use only. No apply on irrited or injured skin.

Discountinue use if you experience some irritation. Redness or discomfort

INDICATIONS & USAGE SECTION

Apply under arm only

Shake before use

INACTIVE INGREDIENT SECTION

Water, PPG-15 steary ether, steareth 2

steareth 21, glyrrhiza globra, sodium ascorbyl phosphate

kaolin, glycerin, trisodium EDTa

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Nivea SatinNivea Satin

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69772-110-012020-01-31C16284748780-19d75b9d0-1828-f424-e053-dadaa90a57ce405385f8-cf51-4a2f-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69772-110-01Nieva Satin50 mL in 1 APPLICATORLIQUID502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69772-110NIEVA SATIN (ALUMINUM CHLOROHYDRATE) LIQUID [GENESIS IMPORTS & EXPORTS LLC]2Legacy NDC, 1 package rows20171228_405385f8-cf51-4a2f-e054-00144ff8d46c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69772-11069772-110-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STEARETH-2153J3F32P58IACT
SODIUM ASCORBYL PHOSPHATE836SJG51DRIACT
KAOLIN24H4NWX5COIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
GLYCERINPDC6A3C0OXIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
EDETATE TRISODIUM420IP921MBIACT
STEARETH-2V56DFE46J5IACT
PPG-15 STEARYL ETHER1II18XLS1LIACT

Source Document#

Source XML · Source PDF

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
616b5f96-23f5-0c9a-e053-2a91aa0ae17f405385f8-cf51-4a2f-e054-00144ff8d46c2017-12-28WarningsExact identifier
spl id: 616b5f96-23f5-0c9a-e053-2a91aa0ae17f
spl set id: 405385f8-cf51-4a2f-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.