ALOE UP COCO-MANGO

Product NDC
61477-221
11-digit product format
614770221
Labeler code
61477
Product ID
61477-221_494fc329-26d7-0b3f-e063-6294a90a3afb
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
Aloe Care International, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-02-18
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 15; 5; 15 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ALOE UP COCO-MANGO
Brand name suffix
SPF-50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100mL
HOMOSALATE15 g/100mL
OCTISALATE5 g/100mL
OCTOCRYLENE15 g/100mL

Harmonized Identifiers#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61477-221-14ALOE UP COCO-MANGOSPF-50118 mL in 1 TUBELOTION1185

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61477-221ALOE UP COCO-MANGO SPF-50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [ALOE CARE INTERNATIONAL, LLC]4Current NDC, Legacy NDC, 1 package rows20240214_8506049f-cb43-4d1d-885b-c6d3a99bbba3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61477-221-1461477022114118 mL in 1 TUBE (61477-221-14) 118 ml2019-02-180000-00-00NoNoCurrent