Manuka Honey Extra Strength
- Product NDC
- 81995-050
- 11-digit product format
- 819950050
- Labeler code
- 81995
- Product ID
- 81995-050_2d5e1f54-b018-fce5-e063-6394a90a76d7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALLANTOIN
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- First Honey LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-09-01
- Substance
- ALLANTOIN
- Active strength
- 5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Manuka Honey Extra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | 5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81995-050-01 | Manuka Honey Extra Strength | 1 in 1 CARTON | GEL | 1 | | 3 |
| 81995-050-01 | Manuka Honey Extra Strength | 21 g in 1 TUBE | GEL | 21 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81995-050 | MANUKA HONEY EXTRA STRENGTH (ALLANTOIN) GEL [FIRST HONEY LLC] | 3 | Current NDC, 2 package rows | 20250206_b742585d-9a0c-489b-b268-590583cfabd1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 81995-050-01 | 81995005001 | 1 TUBE in 1 CARTON (81995-050-01) / 21 g in 1 TUBE | 1 tube | 2024-09-01 | No | No | Current |