FDA.reportPublic FDA data

Freegells Cough Drops Menthol Eucalyptus

Product NDC
71165-012
11-digit product format
711650012
Labeler code
71165
Product ID
71165-012_08a1d725-5476-d285-e063-6294a90addc0
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
LOZENGE
Route
ORAL
Labeler
Riclan S.A.
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-10-01
Substance
MENTHOL
Active strength
5.4 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Freegells Cough Drops Menthol Eucalyptus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL5.4 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui485287

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71165-012-00Freegells Cough Drops Menthol Eucalyptus30 in 1 BAGLOZENGE302
71165-012-01Freegells Cough Drops Menthol Eucalyptus80 in 1 BAGLOZENGE802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71165-012FREEGELLS COUGH DROPS MENTHOL EUCALYPTUS (MENTHOL) LOZENGE [RICLAN S.A.]2Current NDC, Legacy NDC, 2 package rows20231027_1141593a-f3ba-4adf-b332-f9fcb0b5a013.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
485287menthol 5.4 MG Oral LozengePSN1141593a-f3ba-4adf-b332-f9fcb0b5a0132
485287menthol 5.4 MG Oral LozengeSCD1141593a-f3ba-4adf-b332-f9fcb0b5a0132

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71165-012-007116500120030 LOZENGE in 1 BAG (71165-012-00) 30 lozenge2022-10-010000-00-00NoNoCurrent
71165-012-017116500120180 LOZENGE in 1 BAG (71165-012-01) 80 lozenge2022-10-010000-00-00NoNoCurrent