DeodorantStick

Manufacturer
Shengnan (Guangzhou) Cosmetics Co., LTD
Effective date
2024-12-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:42:45

Label at a glance#

ProductDeodorantStick
Active ingredientBUTYROSPERMUM PARKII (SHEA) BUTTER
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

avoid danger of suffocation, keep this bag away from babies and children.

OTC - PURPOSE SECTION

Deodorant

OTC - STOP USE SECTION

Stop use and ask doctor if rash occurs.

OTC - ACTIVE INGREDIENT SECTION

BUTYROSPERMUM PARKII (SHEA) BUTTER

OTC - WHEN USING SECTION

Do not apply to wounds or damaged skin.

INACTIVE INGREDIENT SECTION

Caprylic/Capric Triglyceride
Glycerin
Beeswax
Ozokerite
Simmondsia Chinensis (Jojoba) Seed Oil
Fragrance
Phenoxyethanol
Tocopherol

DOSAGE & ADMINISTRATION SECTION

Apply 1-2 times a day

INDICATIONS & USAGE SECTION

Releases a long-lasting fragrance on the skin.
creating a pleasant aroma around the body

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84019-013-01DeodorantStick45 g in 1 BOTTLECREAM451

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84019-013DEODORANTSTICK (MAGNESIUM HYDROXIDE) CREAM [SHENGNAN (GUANGZHOU) COSMETICS CO., LTD]11 package rows20241215_286f7e2f-94d2-22b5-e063-6394a90a3ad5.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84019-01384019-013-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

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
286f7e2f-94d3-22b5-e063-6394a90a3ad5286f7e2f-94d2-22b5-e063-6394a90a3ad52024-12-04WarningsExact identifier
spl id: 286f7e2f-94d3-22b5-e063-6394a90a3ad5
spl set id: 286f7e2f-94d2-22b5-e063-6394a90a3ad5

Reported adverse events (FAERS/openFDA)#

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