NATURAL LIQUIDMINERALSPRAY
- Product NDC
- 87034-0002
- 11-digit product format
- 870340002
- Labeler code
- 87034
- Product ID
- 87034-0002_3d26d608-27b3-86f3-e063-6394a90abd83
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- K-LA-KO Co.,LTD
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-06-01
- Substance
- SODIUM CHLORIDE
- Active strength
- 100 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 451W47IQ8X | SODIUM CHLORIDE | 7647-14-5 | SODIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87034-0002-1 | 87034000201 | 100 mL in 1 BOTTLE, SPRAY (87034-0002-1) | 100 ml | 2025-06-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | K-LA-KO Co.,LTD | 2025-08-24 | HUMAN OTC DRUG LABEL | 1 |