KONEUK SUNSCREEN SPF50
- Product NDC
- 84167-323
- 11-digit product format
- 841670323
- Labeler code
- 84167
- Product ID
- 84167-323_48dd7f6e-2a4e-2c92-e063-6294a90a4255
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- KONEUK SUNSCREEN SPF50
- Dosage form
- CREAM
- Route
- CUTANEOUS
- Labeler
- Guangzhou Meixi Biotechnology Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-21
- Substance
- AVOBENZONE; ENSULIZOLE; HOMOSALATE; OCTOCRYLENE; TITANIUM DIOXIDE
- Active strength
- 1; 1; 1; 1; 1 g/1; g/1; g/1; g/1; g/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84167-323-03 | KONEUK SUNSCREEN SPF50 | 5 in 1 BOX | CREAM | 5 | | 1 |
| 84167-323-03 | KONEUK SUNSCREEN SPF50 | 1 in 1 BOTTLE | CREAM | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84167-323-03 | 84167032303 | 5 BOTTLE in 1 BOX (84167-323-03) / 1 CREAM in 1 BOTTLE | 5 bottle | 2026-01-21 | No | No | Historical |