DRY GRIP PDP

Manufacturer
Chongqing Alefa Technology Co., Ltd.
Effective date
2026-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:54:44

Label at a glance#

ProductPURE DRY
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

For external use only.
Do not use on broken skin.
Ask a doctor before use if you have kidney disease.
Stop use if rash or irritation occurs.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PURPOSE SECTION

Antiperspirant, apply to underarms only

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 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 drypure dry

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85751-003-01PURE DRY60 g in 1 BOTTLELIQUID601
85751-003-02PURE DRY1 in 1 BOXLIQUID11

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
85751-00385751-003-01, 85751-003-02

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
PURE DRYALUMINUM CHLOROHYDRATEChongqing Alefa Technology Co., Ltd.501b214a-bebe-9956-e063-6394a90a25d02026-04-23WarningsExact identifier
ndc (package): 85751-003-02
ndc (package): 85751-003-01
ndc (product): 85751-003
ndc11 (package): 85751000301
ndc11 (package): 85751000302
spl id: 501b2a48-eacc-8f55-e063-6394a90a7f3e
spl set id: 501b214a-bebe-9956-e063-6394a90a25d0

Reported adverse events (FAERS/openFDA)#

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