EradiKate ACNE TREATMENT

Product NDC
72204-901
11-digit product format
722040901
Labeler code
72204
Product ID
72204-901_44eba48d-5fc8-38ea-e063-6394a90ad2e9
Type
HUMAN OTC DRUG
Nonproprietary name
SULFUR
Dosage form
LIQUID
Route
TOPICAL
Labeler
Rare Beauty Brands Inc
Application
M006
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-06-15
Substance
SULFUR
Active strength
10 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
EradiKate ACNE TREATMENT
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR10 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii70FD1KFU70
Rxcui198869

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72204-901-01EradiKate ACNE TREATMENT30 mL in 1 BOTTLE, GLASSLIQUID309
72204-901-02EradiKate ACNE TREATMENT1 in 1 BOXLIQUID19

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198869sulfur 10 % Topical SolutionPSN44ebacf3-52c1-4896-e063-6394a90ac4479
198869sulfur 100 MG/ML Topical SolutionSCD44ebacf3-52c1-4896-e063-6394a90ac4479
198869sulfur 10 % Topical SolutionSY44ebacf3-52c1-4896-e063-6394a90ac4479

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72204-901-017220409010130 mL in 1 BOTTLE, GLASS30 mlHistorical
72204-901-02722040901021 BOTTLE, GLASS in 1 BOX (72204-901-02) / 30 mL in 1 BOTTLE, GLASS (72204-901-01) 2014-06-15NoNoCurrent