Triple X-Lotion
- Product NDC
- 80724-201
- 11-digit product format
- 807240201
- Labeler code
- 80724
- Product ID
- 80724-201_b1aae991-7767-14aa-e053-2a95a90af462
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Glycolic Acid, Sulfur, Salicylic Acid
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- EMS TRADE
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-10-15
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID; GLYCOLIC ACID; SULFUR
- Active strength
- 1 g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80724-201-01 | Triple X-Lotion | 30 mL in 1 TUBE | LOTION | 30 | | 2 |
| 80724-201-02 | Triple X-Lotion | 60 mL in 1 TUBE | LOTION | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80724-201 | TRIPLE X-LOTION (GLYCOLIC ACID, SULFUR, SALICYLIC ACID) LOTION [EMS TRADE] | 2 | Legacy NDC, 2 package rows | 20231212_b1aae991-7766-14aa-e053-2a95a90af462.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80724-201-01 | 80724020101 | 30 mL in 1 TUBE (80724-201-01) | 30 ml | 2020-10-15 | 0000-00-00 | No | No | Current |
| 80724-201-02 | 80724020102 | 60 mL in 1 TUBE (80724-201-02) | 60 ml | 2020-10-15 | 0000-00-00 | No | No | Current |