Kali Sulf. Bath Essence
- Product NDC
- 48951-6005
- 11-digit product format
- 489516005
- Labeler code
- 48951
- Product ID
- 48951-6005_e3cafac5-b3cb-4454-8237-c0af3d9bd2e3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kali Sulf. Bath Essence
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM SULFIDE
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-6005-6 | Kali Sulf. Bath Essence | 125 mL in 1 BOTTLE, GLASS | LIQUID | 125 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-6005 | KALI SULF. BATH ESSENCE LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20140821_efeb9f62-f328-4d77-8cb3-e4c96fab621e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-6005-6 | 48951600506 | 125 mL in 1 BOTTLE, GLASS | 125 ml | Historical |