Warnings
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.
Pure Dry Liquid
FDA Label NDC 85751-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Chongqing Alefa Technology Co., Ltd. for the product Pure Dry (NDC 85751-002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding warnings, otc - keep out of reach of children, otc - purpose, otc - active ingredient, inactive ingredient, indications & usage, dosage & administration, dry grip pdp, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
antiperspirant for hands & feet
Otc - Active Ingredient
Aluminum Chloride 15%(9g/60ml)
Inactive Ingredient
Purified Water, Glycerin, Hydroxyethylcellulose, Phenoxyethanol, Ethylhexylglycerin, Allantoin, Aloe Barbadensis Leaf Juice Powder
Indications & Usage
Reduces underarm wetness.
Dosage & Administration
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
Pure Dry (1111)
* Please review the disclaimer below.
