FDA.reportPublic FDA data

KINLO Golden Rays Sunscreen (Medium Tinted)

Product NDC
82184-1173
11-digit product format
821841173
Labeler code
82184
Product ID
82184-1173_2b474e64-b832-7742-e063-6294a90afe5c
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
2022-03-08
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 (Medium Tinted)
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC OXIDE132 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiSOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82184-1173-1KINLO Golden Rays Sunscreen (Medium Tinted)28 mL in 1 BOTTLE, PUMPLOTION282
82184-1173-2KINLO Golden Rays Sunscreen (Medium Tinted)1 in 1 CARTONLOTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82184-1173KINLO GOLDEN RAYS SUNSCREEN (MEDIUM TINTED) (ZINC OXIDE) LOTION [A-FRAME SUNCO INC]2Current NDC, Legacy NDC, 2 package rows20250112_d9b57ab5-32c0-6f57-e053-2a95a90a206e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82184-1173-18218411730128 mL in 1 BOTTLE, PUMP28 mlHistorical
82184-1173-2821841173021 BOTTLE, PUMP in 1 CARTON (82184-1173-2) / 28 mL in 1 BOTTLE, PUMP (82184-1173-1) 2022-03-080000-00-00NoNoCurrent