Sunscreen
- Product NDC
- 87243-123
- 11-digit product format
- 872430123
- Labeler code
- 87243
- Product ID
- 87243-123_44136f78-878a-8185-e063-6394a90ad848
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Japanese Sunscreen SPF 50 Super Water Gel Sunscreen 4.22floz(125g) Refill
- Dosage form
- CREAM
- Route
- CUTANEOUS
- Labeler
- MAIDORA CO.,LTD
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-11-21
- Substance
- OCTINOXATE
- Active strength
- 1 g/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTINOXATE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87243-123-35 | Sunscreen | 5 in 1 BOX | CREAM | 5 | | 1 |
| 87243-123-35 | Sunscreen | 1 in 1 CANISTER | CREAM | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87243-123-35 | 87243012335 | 5 CANISTER in 1 BOX (87243-123-35) / 1 CREAM in 1 CANISTER | 5 canister | 2025-11-21 | No | No | Current |