Teevodar

Product NDC
69435-1301
11-digit product format
694351301
Labeler code
69435
Product ID
69435-1301_482fcdd0-6d19-7b96-e063-6294a90a75f1
Type
HUMAN OTC DRUG
Nonproprietary name
Allantoin
Dosage form
CREAM
Route
TOPICAL
Labeler
PEER PHARM LTD.
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-05-15
Substance
ALLANTOIN
Active strength
.5 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Teevodar
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALLANTOIN.5 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii344S277G0Z
Rxcui241509

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69435-1301-1Teevodar30 g in 1 TUBECREAM303
69435-1301-1Teevodar1 in 1 CARTONCREAM13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69435-1301TEEVODAR (ALLANTOIN) CREAM [PEER PHARM LTD.]2Current NDC, 2 package rows20241227_57a1b6d1-9439-462b-aeb9-ef806e572eaf.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
241509allantoin 0.5 % Topical CreamPSN57a1b6d1-9439-462b-aeb9-ef806e572eaf3
241509allantoin 5 MG/ML Topical CreamSCD57a1b6d1-9439-462b-aeb9-ef806e572eaf3
241509allantoin 0.5 % Topical CreamSY57a1b6d1-9439-462b-aeb9-ef806e572eaf3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69435-1301-1694351301011 TUBE in 1 CARTON (69435-1301-1) / 30 g in 1 TUBE1 tube2023-05-15NoNoHistorical