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EXPORT ONLY - Caudalie Acne-Prone Skin Essentials

Manufacturer
Fareva Morton Grove, Inc.
Effective date
2026-04-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-07-23 05:10:03

Label at a glance#

ProductCaudalie Acne-Prone Skin Essentials
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

For the treatment/management of acne Helps treat acne pimples and allows skin to heal Helps prevent new acne pimples from forming

Dosage and administration

Adults and children 12 years and older: Cleanse skin thoroughly before applying product. For New Users: Apply product to a small area once a day for three days to test if you are sensitive to this product. • If no discomfort occurs, cover the entire affected area with a thin layer. • Start with one application daily, then gradually increase to two or three times daily, if needed. • If dryness or peeling occurs, re...

Label contents#

Full prescribing information#

Medicinal ingredient (w/w)

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 0.5%

Uses

INDICATIONS & USAGE SECTION

For the treatment/management of acne

Helps treat acne pimples and allows skin to heal

Helps prevent new acne pimples from forming

Warnings

WARNINGS SECTION

For external use only as directed.

Allergy alertget medical help right away if you develop hives, swelling of eyes and mouth, blistering, or difficulty breathing.

Ask a doctor before use if you

OTC - ASK DOCTOR SECTION

have severe acne.

When using this product

OTC - WHEN USING SECTION

  • skin irritation and dryness are more likely to occur when using another topical acne product at the same time. If irritation occurs, use only one product at a time
  • avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you develop severe irritation, burning or itching of the skin.
  • improvement is not apparent within 6-8 weeks.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a poison control center or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12 years and older: Cleanse skin thoroughly before applying product. For New Users: Apply product to a small area once
    a day for three days to test if you are sensitive to this product. • If no discomfort occurs, cover the entire affected area with a thin layer. • Start with one application daily, then gradually increase to two or three times daily, if needed. • If dryness or peeling occurs, reduce application to once a day or every other day.

Non-medicinal ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Aqua/Water/Eau, Butylene Glycol, Citral, Citric Acid, Citronellol, Cymbopogon Citratus Leaf Oil, Geraniol, Gluconolactone, Helianthus Annuus (Sunflower) Seed Oil, Lavandula Hybrida Oil, Limonene, Linalool, Melissa Officinalis Leaf Oil, Mentha Piperita (Peppermint) Oil, Niacinamide, Palmitoyl Grape Seed Extract, Pelargonium Graveolens Flower Oil, Rosa Damascena Flower Water, Rosmarinus Officinalis (Rosemary) Leaf Oil, Sodium Citrate, Sodium Hyaluronate, Sodium Hydroxide, Sodium Phytate, Triethyl Citrate, Tocopherol, Xanthan Gum

Questions?

OTC - QUESTIONS SECTION

1-866-826-1615

Package Labeling: Kit

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KitKit

Kit LabelKit Label

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer LabelOuter LabelInner LabelInner Label

AcneSerum11AcneSerum11

Label - Insert0Label - Insert0

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeITF23617590000627GTIN-14: 23617590000627
GTIN storage (14 digits): 23617590000627		Kit Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72686-10772686-107-31
72686-10072686-100-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CITRALT7EU0O9VPPIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
WEST INDIAN LEMONGRASS OIL5BIA40E9EDIACT
GERANIOLL837108USYIACT
GLUCONOLACTONEWQ29KQ9POTIACT
SUNFLOWER OIL3W1JG795YIIACT
LAVANDIN OIL9RES347CKGIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
MELISSA OFFICINALIS LEAF OILPTP6R7263MIACT
PEPPERMINT OILAV092KU4JHIACT
NIACINAMIDE25X51I8RD4IACT
PALMITOYL VITIS VINIFERA SEED PROANTHOCYANIDINSZZE3L9H7KHIACT
PELARGONIUM GRAVEOLENS FLOWER OIL3K0J1S7QGCIACT
ROSA X DAMASCENA FLOWER OIL18920M3T13IACT
ROSEMARY OIL8LGU7VM393IACT
SODIUM CITRATE, UNSPECIFIED FORM1Q73Q2JULRIACT
SODIUM HYALURONATEYSE9PPT4THIACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM PHYTATE88496G1ERLIACT
TRIETHYL CITRATE8Z96QXD6UMIACT
TOCOPHEROLR0ZB2556P8IACT
XANTHAN GUMTTV12P4NEEIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4ff4cc23-0d1f-8446-e063-6294a90a92d79ecee917-e480-4527-b8d0-91e73ae0a8152026-04-21WarningsExact identifier
spl id: 4ff4cc23-0d1f-8446-e063-6294a90a92d7
spl set id: 9ecee917-e480-4527-b8d0-91e73ae0a815

Reported adverse events (FAERS/openFDA)#

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