Hydra Finish SPF 15

Product NDC
54181-006
11-digit product format
541810006
Labeler code
54181
Product ID
54181-006_498dad38-0a60-0ca1-e063-6394a90ab995
Type
HUMAN OTC DRUG
Nonproprietary name
HOMOSALATE, OCTINOXATE
Dosage form
CREAM
Route
TOPICAL
Labeler
Guinot
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-07-22
Substance
HOMOSALATE; OCTINOXATE
Active strength
40; 60 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Hydra Finish SPF 15
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOMOSALATE40 mg/mL
OCTINOXATE60 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV06SV4M95S, 4Y5P7MUD51

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54181-006-30Hydra Finish SPF 151 in 1 CARTONCREAM110
54181-006-30Hydra Finish SPF 1530 mL in 1 TUBECREAM3010

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54181-006HYDRA FINISH SPF 15 (HOMOSALATE, OCTINOXATE) CREAM [GUINOT]9Current NDC, Legacy NDC, 2 package rows20240327_4047e8ec-834a-41e6-a144-5649a7718de4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54181-006-30541810006301 TUBE in 1 CARTON (54181-006-30) / 30 mL in 1 TUBE1 tube2016-07-220000-00-00NoNoCurrent