KINLO Golden Rays Sunscreen
- Product NDC
- 82184-4480
- 11-digit product format
- 821844480
- Labeler code
- 82184
- Product ID
- 82184-4480_2b4787da-c1fa-234b-e063-6394a90ad479
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- A-Frame SunCo Inc
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-08-26
- Substance
- ZINC OXIDE
- Active strength
- 132 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- KINLO Golden Rays Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 132 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
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 | Current NDC, 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82184-4480-1 | 82184448001 | 50 mL in 1 BOTTLE, PUMP | 50 ml | | | | | Historical |
| 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 |