Nasal Dryness Relief Gel
- Product NDC
- 10738-051
- 11-digit product format
- 107380051
- Labeler code
- 10738
- Product ID
- 10738-051_49655e27-0a67-4fca-e063-6294a90a5cfa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Genuine Virgin Aloe Corporation
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-05-20
- Substance
- ALLANTOIN
- Active strength
- .5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nasal Dryness Relief Gel
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | .5 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
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 |
|---|
| 10738-051-10 | Nasal Dryness Relief Gel | 1 in 1 CARTON | GEL | 1 | | 2 |
| 10738-051-15 | Nasal Dryness Relief Gel | 28 g in 1 TUBE | GEL | 28 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10738-051-10 | 10738005110 | 1 TUBE in 1 CARTON (10738-051-10) / 28 g in 1 TUBE (10738-051-15) | 1 tube | 2022-05-20 | No | No | Historical |
| 10738-051-15 | 10738005115 | 28 g in 1 TUBE | 28 g | | | | Historical |