Rohto
- Product NDC
- 10742-8459
- 11-digit product format
- 107428459
- Labeler code
- 10742
- Product ID
- 10742-8459_29aaa211-07f2-71e1-e063-6294a90a1e43
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hypromellose, Povidone
- Dosage form
- LIQUID
- Route
- OPHTHALMIC
- Labeler
- The Mentholatum Company
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-05-30
- Substance
- HYPROMELLOSE, UNSPECIFIED; POVIDONE
- Active strength
- 3; 5 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Rohto
- Brand name suffix
- Dual Light Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYPROMELLOSE, UNSPECIFIED | 3 mg/mL |
| POVIDONE | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3NXW29V3WO, FZ989GH94E |
| Rxcui | 2604775 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10742-8459-1 | RohtoDual Light Relief | 18 mL in 1 BOTTLE, DISPENSING | LIQUID | 18 | | 3 |
| 10742-8459-1 | RohtoDual Light Relief | 1 in 1 CARTON | LIQUID | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10742-8459 | ROHTO DUAL LIGHT RELIEF (HYPROMELLOSE, POVIDONE) LIQUID [THE MENTHOLATUM COMPANY] | 3 | Current NDC, 2 package rows | 20241222_1b597f83-d7f1-cf93-e063-6394a90a99f7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 10742-8459-1 | 10742845901 | 1 BOTTLE, DISPENSING in 1 CARTON (10742-8459-1) / 18 mL in 1 BOTTLE, DISPENSING | 2024-05-30 | No | No | Historical |