FDA.reportPublic FDA data

Alocane Advanced Scar and Itch

Product NDC
68229-409
11-digit product format
682290409
Labeler code
68229
Product ID
68229-409_26301c2d-6d14-ec1d-e063-6394a90ac524
Type
HUMAN OTC DRUG
Nonproprietary name
Calendula Officinalis, Grindelia Robusta
Dosage form
GEL
Route
TOPICAL
Labeler
Quest Products, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-11-05
Substance
CALENDULA OFFICINALIS FLOWER; GRINDELIA HIRSUTULA FLOWERING TOP
Active strength
1; 1 [hp_X]/20.7mL; [hp_X]/20.7mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Alocane Advanced Scar and Itch
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CALENDULA OFFICINALIS FLOWER1 [hp_X]/20.7mL
GRINDELIA HIRSUTULA FLOWERING TOP1 [hp_X]/20.7mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiP0M7O4Y7YD, IDB0NAZ6AI

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68229-409-01Alocane Advanced Scar and Itch20.7 mL in 1 TUBEGEL20.71
68229-409-02Alocane Advanced Scar and Itch1 in 1 CARTONGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68229-409ALOCANE ADVANCED SCAR AND ITCH (CALENDULA OFFICINALIS, GRINDELIA ROBUSTA) GEL [QUEST PRODUCTS, LLC]1Current NDC, 2 package rows20241109_26301c2d-6d13-ec1d-e063-6394a90ac524.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
68229-409-016822904090120.7 mL in 1 TUBE20.7 mlHistorical
68229-409-02682290409021 TUBE in 1 CARTON (68229-409-02) / 20.7 mL in 1 TUBE (68229-409-01) 1 tube2024-11-05NoNoCurrent