FDA.reportPublic FDA data

Chiggerex

Product NDC
52412-350
11-digit product format
524120350
Labeler code
52412
Product ID
52412-350_297a5049-0d6d-4e96-e063-6294a90a557d
Type
HUMAN OTC DRUG
Nonproprietary name
Benzocaine
Dosage form
CREAM
Route
TOPICAL
Labeler
RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-02-01
Substance
BENZOCAINE
Active strength
.1 g/g
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Chiggerex
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOCAINE.1 g/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3RSY48JW5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52412-350-17Chiggerex170 g in 1 JARCREAM1702
52412-350-50Chiggerex50 g in 1 JARCREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52412-350CHIGGEREX (BENZOCAINE) CREAM [RANDOB LABS, LTD. DBA CROSSINGWELL CONSUMER HEALTH]2Current NDC, Legacy NDC, 2 package rows20241219_5e5d84ab-f57f-448d-a4c1-ced38890eec2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52412-350-1752412035017170 g in 1 JAR (52412-350-17) 170 g2022-02-01NoNoCurrent
52412-350-505241203505050 g in 1 JAR (52412-350-50) 50 g2020-02-010000-00-00NoNoCurrent