Droptics Dry Eye Relief
- Product NDC
- 85211-002
- 11-digit product format
- 852110002
- Labeler code
- 85211
- Product ID
- 85211-002_49dd075b-e16b-f725-e063-6294a90ad952
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carboxymethylcellulose Sodium,Glycerin,Polysorbate 80
- Dosage form
- LIQUID
- Route
- OPHTHALMIC
- Labeler
- Droptics LLC
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-02-01
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80
- Active strength
- .5; 1; .5 g/100mL; g/100mL; g/100mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Droptics Dry Eye Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBOXYMETHYLCELLULOSE SODIUM | .5 g/100mL |
| GLYCERIN | 1 g/100mL |
| POLYSORBATE 80 | .5 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K679OBS311, PDC6A3C0OX, 6OZP39ZG8H |
| Rxcui | 1241471 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85211-002-01 | Droptics Dry Eye Relief | 1 in 1 CARTON | LIQUID | 1 | | 3 |
| 85211-002-01 | Droptics Dry Eye Relief | 5 mL in 1 BOTTLE, DROPPER | LIQUID | 5 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 85211-002-01 | 85211000201 | 1 BOTTLE, DROPPER in 1 CARTON (85211-002-01) / 5 mL in 1 BOTTLE, DROPPER | 2025-02-01 | No | No | Current |