DRY GRIP PDP

Manufacturer: Chongqing Alefa Technology Co., Ltd.
Effective date: 2026-04-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:54:39

Label at a glance#

ProductPURE DRY

Active ingredientALUMINUM CHLORIDE

Label structure8 sections

Label contents#

Full prescribing information#

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.

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

Purified Water, Glycerin, Hydroxyethylcellulose, Phenoxyethanol, Ethylhexylglycerin, Allantoin, Aloe Barbadensis Leaf Juice Powder

INDICATIONS & USAGE SECTION

Reduces underarm wetness.

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.
Apply at bedtime to clean, fully dry underarms.
Apply sparingly — only a few strokes under each arm.
Do not apply immediately after shaving or on irritated skin.
For sensitive skin: start 2–3 nights per week, then increase as needed.
Let dry before dressing.

DRY GRIP PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pure dry

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85751-002-01	PURE DRY	60 g in 1 BOTTLE	LIQUID	60		1
85751-002-02	PURE DRY	1 in 1 BOX	LIQUID	1		1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

PURE DRY
Aluminum Chloride
WATER
GLYCERIN
HYDROXYETHYLCELLULOSE
ALUMINUM CATION
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
ALLANTOIN
ALOE BARBADENSIS LEAF JUICE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85751-002	85751-002-01, 85751-002-02

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
HYDROXYETHYLCELLULOSE	T4V6TWG28D	IACT
ALUMINUM CHLORIDE	3CYT62D3GA	ACTIB
PHENOXYETHANOL	HIE492ZZ3T	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
ALLANTOIN	344S277G0Z	IACT
ALOE BARBADENSIS LEAF JUICE	RUE8E6T4NB	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PURE DRY	ALUMINUM CHLORIDE	Chongqing Alefa Technology Co., Ltd.	500d4d04-3765-4d58-e063-6394a90a6dc2	2026-04-22	Warnings	Exact identifier ndc (package): 85751-002-01 ndc (package): 85751-002-02 ndc (product): 85751-002 ndc11 (package): 85751000202 ndc11 (package): 85751000201 spl id: 500d4d13-2714-5b76-e063-6294a90ac763 spl set id: 500d4d04-3765-4d58-e063-6394a90a6dc2

Reported adverse events (FAERS/openFDA)#

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