SUNSCREEN LIP PROTECTIONBROAD SPECTRUM SPF 15

Product NDC
84066-103
11-digit product format
840660103
Labeler code
84066
Product ID
84066-103_46871df7-0e77-a3c4-e063-6394a90a82c5
Type
HUMAN OTC DRUG
Nonproprietary name
Ethylhexyl Methoxycinnamate, Octocrylene
Dosage form
GEL
Route
TOPICAL
Labeler
Guangzhou Tata Biotechnology Co., Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-07-02
Substance
OCTINOXATE; OCTOCRYLENE
Active strength
7.5; 5 mg/100mL; mg/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SUNSCREEN LIP PROTECTIONBROAD SPECTRUM SPF 15
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE7.5 mg/100mL
OCTOCRYLENE5 mg/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84066-103-01SUNSCREEN LIP PROTECTIONBROAD SPECTRUM SPF 1510 mL in 1 TUBEGEL104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84066-103SUNSCREEN LIP PROTECTIONBROAD SPECTRUM SPF 15 (ETHYLHEXYL METHOXYCINNAMATE, OCTOCRYLENE) GEL [GUANGZHOU TATA BIOTECHNOLOGY CO., LTD.]2Current NDC, 1 package rows20240723_1c32b019-a038-eb61-e063-6394a90a45f2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84066-103-018406601030110 mL in 1 TUBE (84066-103-01) 10 ml2024-07-02NoNoHistorical