DRY GRIP

Manufacturer
Chongqing Alefa Technology Co., Ltd.
Effective date
2025-06-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:02:16

Label at a glance#

ProductDRY GRIP
Active ingredientALUMINUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION


Antiperspirant for Hands & Feet.
Apply at night to clean, dry skin.
Spray evenly on hands or feet.
Let dry completely before covering or sleeping.
Wash off in the morning.
Use nightly for 2–3 days, then 1–2 times weekly as needed.

WARNINGS SECTION


For external use only.
Do not use on broken or recently shaved skin.
Avoid contact with eyes or mouth.
Stop use if irritation or rash occurs.
Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION


Apply to clean, dry hands and/or feet once daily.
Use preferably at bedtime.
Allow to dry completely before covering skin or putting on socks/shoes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PURPOSE SECTION


antiperspirant for hands & feet

OTC - ACTIVE INGREDIENT SECTION


Aluminum Chloride 15%(9g/60ml)

INACTIVE INGREDIENT SECTION

Water, Alcohol Denat, Propylene Glycol, Hamamelis Virginiana Extract, Aloe Barbadensis Leaf Juice, Glycerin, Allantoin, Phenoxyethanol

DRY GRIP PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85751-001-01DRY GRIP60 g in 1 BOTTLE, SPRAYSPRAY, METERED601
85751-001-01DRY GRIP1 in 1 BOXSPRAY, METERED11

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
85751-00185751-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
DRY GRIPALUMINUM CHLORIDEChongqing Alefa Technology Co., Ltd.36a79c9d-27bc-78f3-e063-6394a90a2da62025-06-03WarningsExact identifier
ndc (package): 85751-001-01
ndc (product): 85751-001
ndc11 (package): 85751000101
spl id: 36a79c9d-27bd-78f3-e063-6394a90a2da6
spl set id: 36a79c9d-27bc-78f3-e063-6394a90a2da6

Reported adverse events (FAERS/openFDA)#

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