PURE DRY
- Product NDC
- 85751-003
- 11-digit product format
- 857510003
- Labeler code
- 85751
- Product ID
- 85751-003_501b2a48-eacc-8f55-e063-6394a90a7f3e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chlorohydrate
- 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 CHLOROHYDRATE
- 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 CHLOROHYDRATE | 15 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HPN8MZW13M |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85751-003-01 | PURE DRY | 60 g in 1 BOTTLE | LIQUID | 60 | | 1 |
| 85751-003-02 | 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 |
|---|
| 85751-003-01 | 85751000301 | 60 g in 1 BOTTLE | 60 g | | | | Historical |
| 85751-003-02 | 85751000302 | 1 BOTTLE in 1 BOX (85751-003-02) / 60 g in 1 BOTTLE (85751-003-01) | 1 bottle | 2026-04-22 | No | No | Current |