Fusion Water Magic

Product NDC
69494-016
11-digit product format
694940016
Labeler code
69494
Product ID
69494-016_8b0f9e3b-5166-4de7-b194-10e02391c196
Type
HUMAN OTC DRUG
Nonproprietary name
Octocrylene, Homosalate, Octisalate, and Avobenzone
Dosage form
LOTION
Route
TOPICAL
Labeler
ISDIN Corp.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-03-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
27; 73; 45; 90 mg/mL; mg/mL; 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
Fusion Water Magic
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE27 mg/mL
HOMOSALATE73 mg/mL
OCTISALATE45 mg/mL
OCTOCRYLENE90 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69494-016-01Fusion Water Magic50 mL in 1 BOTTLE, PLASTICLOTION504
69494-016-01Fusion Water Magic1 in 1 CARTONLOTION14
69494-016-02Fusion Water Magic10 mL in 1 BOTTLE, PLASTICLOTION104
69494-016-02Fusion Water Magic1 in 1 CARTONLOTION14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69494-016FUSION WATER MAGIC (OCTOCRYLENE, HOMOSALATE, OCTISALATE, AND AVOBENZONE) LOTION [ISDIN CORP.]1Current NDC, 4 package rows20250101_d4f91d5a-600a-4255-a6e1-e7e7197848c7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
69494-016-01694940016011 BOTTLE, PLASTIC in 1 CARTON (69494-016-01) / 50 mL in 1 BOTTLE, PLASTIC2025-02-15NoNoCurrent
69494-016-02694940016021 BOTTLE, PLASTIC in 1 CARTON (69494-016-02) / 10 mL in 1 BOTTLE, PLASTIC2025-02-15NoNoCurrent