PURE DRY
- Product NDC
- 85751-002
- 11-digit product format
- 857510002
- Labeler code
- 85751
- Product ID
- 85751-002_500d4d13-2714-5b76-e063-6294a90ac763
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Chongqing Alefa Technology Co., Ltd.
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-22
- Substance
- ALUMINUM CHLORIDE
- Active strength
- 15 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PURE DRY
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLORIDE | 15 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3CYT62D3GA |
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 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85751-002-01 | 85751000201 | 60 g in 1 BOTTLE | 60 g | | | | Historical |
| 85751-002-02 | 85751000202 | 1 BOTTLE in 1 BOX (85751-002-02) / 60 g in 1 BOTTLE (85751-002-01) | 1 bottle | 2026-04-22 | No | No | Current |