Quita Callos Corn and Callus Remover

Product NDC
73635-5811
11-digit product format
736355811
Labeler code
73635
Product ID
73635-5811_5d6d88d8-a9b2-9245-e063-6294a90a3c55
Type
HUMAN OTC DRUG
Nonproprietary name
Salisylic Acid 17%
Dosage form
LIQUID
Route
TOPICAL
Labeler
Germa Products, LLC
Application
M030
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-03-29
Substance
SALICYLIC ACID
Active strength
170 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct73635-5811DDiscontinued by firm2026-10-15
excluded packagepackage73635-581173635-5811-5DDiscontinued by firm2026-10-15

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage73635-5811-5d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage73635-5811-5f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage73635-5811-52ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage73635-5811-5a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage73635-5811-5cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage73635-5811-5cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage73635-5811-5302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage73635-5811-5ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage73635-5811-50efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage73635-5811-5ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage73635-5811-5367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage73635-5811-5557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Quita Callos Corn and Callus Remover
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID170 mg/mL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73635-5811-5Quita Callos Corn and Callus Remover14.8 mL in 1 BOTTLE, WITH APPLICATORLIQUID14.86
73635-5811-5Quita Callos Corn and Callus Remover1 in 1 BOXLIQUID16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73635-5811QUITA CALLOS CORN AND CALLUS REMOVER (SALISYLIC ACID 17%) LIQUID [GERMA PRODUCTS, LLC]5Current NDC, Legacy NDC, 2 package rows20241017_bf783cd0-e814-11e2-e053-2995a90a7015.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 4 of 5 · 99 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Salicylic AcidMEDICATED CALLUS REMOVERSDiscount Drug Martf9ccb61c-e7cb-442c-aca9-f2ce6b4a4e432025-12-29WarningsExact identifier
application number: M030
Scholls Wellness Company LLC One Step Corn RemoversSALICYLIC ACIDScholls Wellness Company LLC7f98d59c-fc89-545b-e053-2a91aa0a49e62025-12-21WarningsExact identifier
application number: M030
Scholls Wellness Company LLC DURAGEL CORN REMOVERSALICYLIC ACIDScholls Wellness Company LLCb7249271-0561-db00-e053-2995a90ac0222025-12-21WarningsExact identifier
application number: M030
Scholls Wellness Company LLC Duragel Callus RemoverSALICYLIC ACIDScholls Wellness Company LLCb7256b0a-3c7e-139f-e053-2a95a90ad3442025-12-21WarningsExact identifier
application number: M030
Scholls Wellness Company LLC DS EXTRA THICK CALLUS REMOVERSALICYLIC ACIDScholls Wellness Company LLCb7144150-6c81-66c2-e053-2995a90ad6e92025-12-21WarningsExact identifier
application number: M030
Foster and Thrive Medicated Corn Removers40% W/W SALICYLIC ACID CORN REMOVERStrategic Sourcing Services LLC1a51a539-e9b5-9dab-e063-6294a90a6cd22025-12-05WarningsExact identifier
application number: M030
Scott Clear Corn Removers40% W/W SALICYLIC ACID CORN REMOVERCreative Foam Corporationdd949b90-2f11-75eb-e053-2995a90af5a52025-12-05WarningsExact identifier
application number: M030
YAT TIP TORSALICYLIC ACIDZhejiang Dingtai Pharmaceutical Co., Ltd085f1e46-4ac1-43af-a15d-880ce017759f2025-11-10WarningsExact identifier
application number: M030
MQXUNMI BEE VENOM CORN CALLUS REMOVERSBEE VENOM CORN CALLUS REMOVERSZhengzhou Miaoqi Medical Technology Co., Ltd.41952a0e-2bd2-db3c-e063-6294a90a4a792025-10-20WarningsExact identifier
application number: M030
MediPlastSALICYLIC ACIDMedline Industries, LP35bd29f9-cf49-404b-826b-72d1269d4f192025-10-13WarningsExact identifier
application number: M030
Compound W One Step Medicated Corn RemoverSALICYLIC ACIDMedtech Products Inc.7ebf39fa-b069-4630-9712-c9996e20cf862025-10-09WarningsExact identifier
application number: M030
Salicylic AcidCORN AND CALLUS REMOVER KITHudson Health LLC74cbc2f4-4d6e-406d-a64e-bd293552d4d82025-10-08WarningsExact identifier
application number: M030
Salicylic AcidLIQUID CORN AND CALLUS REMOVERFSA Store Inc.3cd18e4c-26c1-1548-e063-6294a90acdb02025-10-08WarningsExact identifier
application number: M030
Salicylic AcidLIQUID CORN AND CALLUS REMOVERFoodhold USA966889e5-65d9-4057-ac7d-0f985e7c67342025-10-08WarningsExact identifier
application number: M030
Liquid Callus RemoverSALICYLIC ACIDPremier Brands of America Inc.051c7917-76ea-c7f8-e063-6394a90a9e362025-10-08WarningsExact identifier
application number: M030
Salicylic AcidCORN AND CALLUS REMOVERGeiss, Destin & Dunn, Inc.21b8d34d-1127-4b0d-b853-0349f25cc91f2025-10-08WarningsExact identifier
application number: M030
Salicylic AcidLIQUID CORN AND CALLUS REMOVERHarris Teeter, LLC27a1c74d-f983-4e18-9854-7a83c3365c852025-10-08WarningsExact identifier
application number: M030
Salicylic AcidCORN AND CALLUS REMOVER KITKroger Co.c63a4d29-76e2-4d20-8671-e01311ca30902025-10-08WarningsExact identifier
application number: M030
Liquid Corn and Callus RemoverSALICYLIC ACIDMeijer Distribution Inc039c3dbe-97ba-805c-e063-6394a90a91e82025-10-08WarningsExact identifier
application number: M030
Salicylic AcidLIQUID CORN AND CALLUS REMOVERWalgreen Company8305ee69-3940-43e8-b6bb-b6438a14ef5c2025-10-08WarningsExact identifier
application number: M030

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312881salicylic acid 17 % Topical SolutionPSNbf783cd0-e814-11e2-e053-2995a90a70156
312881salicylic acid 170 MG/ML Topical SolutionSCDbf783cd0-e814-11e2-e053-2995a90a70156
312881salicylic acid 17 % Topical SolutionSYbf783cd0-e814-11e2-e053-2995a90a70156

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
73635-5811-5736355811051 BOTTLE, WITH APPLICATOR in 1 BOX (73635-5811-5) / 14.8 mL in 1 BOTTLE, WITH APPLICATOR2019-03-290000-00-00NoNoCurrent