FDA.reportPublic FDA data

Keeva Organics Acne Treatment Cream Salicylic Acid

Manufacturer
COB Ecommerce Empire LLC
Effective date
2019-08-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:14:51

Label at a glance#

ProductKeeva Organics Acne Treatment
Active ingredientSALICYLIC ACID
Label structure6 sections

Dosage and administration

clean the skin thoroughly before applying this product cover the entire affected area with a thin layer one to three times daily because excessive drying of the skin may occur, start with one application aily, then gradually increase to two or three times daily if needed or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day if going outside, apply s...

Label contents#

Full prescribing information#

Proprietary Ingredients

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 10% w/v

OTC - PURPOSE SECTION

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Stearic Acid, Glyceryl Stearate, She Butter, Rosehip Seed Oil, Sesame Seed Oil, Olive Oil, Extracts of White Willows, Burdock, Milk Thistle, Hops, Sophora Root Extract, Squalene, Isooctyl Palmitate, Ispropyl Myristate, Polydimethylsiloxane, Salicylic Acid, Vitamin E, tea Tree Oil, Argan Oil, Phenoxyethanol, DL-Menthol, Hyaluronic Acid, and Grapeseed Extract.

Use

INDICATIONS & USAGE SECTION

acne treatment

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if you • have sensitive skin • are sensitive to salicylic acid

When using this product

OTC - WHEN USING SECTION

  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
  • rinse right away with water if it gets in eyes avoid unnecessary sun exposure and use a sunscreen
  • avoid contact with the eyes, lips and mouth
  • avoid contact with hair and dyed fabrics, which maybe bleached by this product
  • skin irritation may occur, characterized by redness, burning, itching, peeling or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Stop use and ask a doctor

OTC - STOP USE SECTION

if skin irritation becomes severe

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application
  • aily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day
  • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor,

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72206-00072206-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STEARIC ACID4ELV7Z65APIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
SHEA BUTTERK49155WL9YIACT
ROSA MOSCHATA OILJ99W255AWFIACT
OLIVE OIL6UYK2W1W1EIACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
MILK THISTLEU946SH95EEIACT
HOPS01G73H6H83IACT
SQUALENE7QWM220FJHIACT
ISOCETYL PALMITATE355356620ZIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
DIMETHICONE92RU3N3Y1OIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
TEA TREE OILVIF565UC2GIACT
ARGAN OIL4V59G5UW9XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
RACEMENTHOLYS08XHA860IACT
HYALURONIC ACIDS270N0TRQYIACT
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML · Source PDF

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
908d959d-32d5-e09d-e053-2a95a90a9a400220ba1d-4bb0-4f3d-9fa5-31329f9e2d982019-08-20WarningsExact identifier
spl id: 908d959d-32d5-e09d-e053-2a95a90a9a40
spl set id: 0220ba1d-4bb0-4f3d-9fa5-31329f9e2d98

Reported adverse events (FAERS/openFDA)#

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