KINLO Golden Rays Sunscreen
- Product NDC
- 82184-4480
- Requested package NDC
- 82184-4480-2
- 11-digit product format
- 821844480
- Labeler code
- 82184
- Product ID
- 82184-4480_cb18e595-9870-6769-e053-2a95a90acfd3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- A-Frame SunCo Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-08-26
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 132 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82184-4480-1 | KINLO Golden Rays Sunscreen | 50 mL in 1 BOTTLE, PUMP | LOTION | 50 | | 2 |
| 82184-4480-2 | KINLO Golden Rays Sunscreen | 1 in 1 CARTON | LOTION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82184-4480 | KINLO GOLDEN RAYS SUNSCREEN (ZINC OXIDE) LOTION [A-FRAME SUNCO INC] | 2 | Legacy NDC, 2 package rows | 20250112_cb18e5c3-e184-7986-e053-2995a90a5c3b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82184-4480-2 | 82184448002 | 1 BOTTLE, PUMP in 1 CARTON (82184-4480-2) > 50 mL in 1 BOTTLE, PUMP (82184-4480-1) | 2021-08-26 | 0000-00-00 | No | No | Current |