Lavender Callus Remover Gel

Manufacturer: SANSAR, LLC
Effective date: 2025-05-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:00:51

Label at a glance#

ProductLavender Callus Remover

Active ingredientSALICYLIC ACID

Label structure10 sections

Indications and uses

for the removal of corns and calluses Relieves pain by removing corns and calluses

Dosage and administration

Soak feet for 10-15 minutes Dry with a towel Wear Gloves, apply callus remover gel, leave for 10-15 minutes. Rinse of residue.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 12%

Purpose

OTC - PURPOSE SECTION

Corn and callus remover

Uses

INDICATIONS & USAGE SECTION

for the removal of corns and calluses
Relieves pain by removing corns and calluses

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on Children under 2 without a Doctor's advice.

When using this product

OTC - WHEN USING SECTION

Wear gloves. Limit use to 20 minutes. Use cautiously with electric filing machines.
Avoid broken or non calloused skin.
Avoid eye contact. Rinse for 15 minutes if contcat occurs. consult a physician if irritation persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Soak feet for 10-15 minutes
Dry with a towel
Wear Gloves, apply callus remover gel, leave for 10-15 minutes.
Rinse of residue.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Distilled water, Alcohol ethoxylate, Potassium Hydroxide, Glycerin, Tetrasodium EDTA, Fragrance Essential Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

lavendar-gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2714099	salicylic acid 12 % Topical Gel	PSN	1
2714099	salicylic acid 0.12 MG/MG Topical Gel	SCD	1
2714099	salicylic acid 12 % Topical Gel	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
83691-012-01	Lavender Callus Remover	236 mL in 1 BOTTLE	GEL	236	1
83691-012-01	Lavender Callus Remover	1 in 1 CARTON	GEL	1	1
83691-012-02	Lavender Callus Remover	236 mL in 1 BOTTLE	GEL	236	1
83691-012-02	Lavender Callus Remover	2 in 1 CARTON	GEL	2	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
83691-012	LAVENDER CALLUS REMOVER (SALICYLIC ACID 12%) GEL [SANSAR, LLC]	1	Current NDC, 4 package rows	20250514_4763bab3-631a-4fcf-8387-d7df4e89e0e4.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

Lavender Callus Remover
Salicylic Acid 12%
SALICYLIC ACID
POTASSIUM HYDROXIDE
GLYCERIN
1-ETHOXYUNDECANE
EDETATE SODIUM
LAVENDER OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83691-012	83691-012-01, 83691-012-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SALICYLIC ACID	O414PZ4LPZ	ACTIB
POTASSIUM HYDROXIDE	WZH3C48M4T	IACT
GLYCERIN	PDC6A3C0OX	IACT
1-ETHOXYUNDECANE	R428J6A8Q2	IACT
EDETATE SODIUM	MP1J8420LU	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lavender Callus Remover	SALICYLIC ACID 12%	SANSAR, LLC	4763bab3-631a-4fcf-8387-d7df4e89e0e4	2025-05-09	Warnings	Exact identifier ndc (package): 83691-012-02 ndc (package): 83691-012-01 ndc (product): 83691-012 ndc11 (package): 83691001202 ndc11 (package): 83691001201 spl id: 7fe066f6-285e-4c55-ba18-64cc70f8d3c5 spl set id: 4763bab3-631a-4fcf-8387-d7df4e89e0e4

Reported adverse events (FAERS/openFDA)#

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