Tukol Max Action
- Product NDC
- 50066-518
- 11-digit product format
- 500660518
- Labeler code
- 50066
- Product ID
- 50066-518_d2a614d3-f9b2-4da8-8c7e-a0993d55cd90
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- oxymetazoline hydrochloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Genomma Lab USA
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-02-12
- Substance
- OXYMETAZOLINE HYDROCHLORIDE
- Active strength
- .5 mg/mL
- Pharmacologic classes
- Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tukol Max Action
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYMETAZOLINE HYDROCHLORIDE | .5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K89MJ0S5VY |
| Rxcui | 1000990 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50066-518-05 | Tukol Max Action | 1 in 1 CARTON | LIQUID | 1 | | 1 |
| 50066-518-05 | Tukol Max Action | 15 mL in 1 BOTTLE, SPRAY | LIQUID | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50066-518 | TUKOL MAX ACTION (OXYMETAZOLINE HYDROCHLORIDE) LIQUID [GENOMMA LAB USA] | 1 | Current NDC, 2 package rows | 20250216_73358103-43dc-4b11-9c89-9a6ba45bf1af.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50066-518-05 | 50066051805 | 1 BOTTLE, SPRAY in 1 CARTON (50066-518-05) / 15 mL in 1 BOTTLE, SPRAY | 2025-02-12 | No | No | Current |