Dr. C. Tuna Sun Stick SPF 50
- Product NDC
- 74690-028
- 11-digit product format
- 746900028
- Labeler code
- 74690
- Product ID
- 74690-028_49dc6085-b934-8106-e063-6394a90a63f9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, OCTINOXATE, HOMOSALATE, OCTOCRYLENE
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- Farmasi US LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-08
- Substance
- AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTOCRYLENE
- Active strength
- 29.5; 73.4; 74.5; 75 mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dr. C. Tuna Sun Stick SPF 50
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 29.5 mg/g |
| HOMOSALATE | 73.4 mg/g |
| OCTINOXATE | 74.5 mg/g |
| OCTOCRYLENE | 75 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4Y5P7MUD51, 5A68WGF6WM |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 74690-028-00 | Dr. C. Tuna Sun Stick SPF 50 | 20 g in 1 BOTTLE, PLASTIC | STICK | 20 | | 1 |
| 74690-028-00 | Dr. C. Tuna Sun Stick SPF 50 | 1 in 1 CARTON | STICK | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 74690-028-00 | 74690002800 | 1 BOTTLE, PLASTIC in 1 CARTON (74690-028-00) / 20 g in 1 BOTTLE, PLASTIC | 2026-01-08 | No | No | Current |