NAELI Exfoliator AHA-BHA Face Cleanser Gel

Manufacturer
ALLI LLC | Pure Source, LLC
Effective date
2025-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:01:21

Label at a glance#

ProductNAELI Exfoliator AHA-BHA Face Cleanser
Active ingredientSALICYLIC ACID
Label structure8 sections

Dosage and administration

Use every morning and evening Wet area first. Apply a dime sized amount to palm and create a lather. Gently massage over the face and neck. Rinse well. May also be used on chest and back. Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily, if needed or as directed by a doctor. If bothersome dryness or peeling occurs, reduce applicat...

Label contents#

Full prescribing information#

Active Ingredient(s)s

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1.00%

Purpose(s)

OTC - PURPOSE SECTION

Acne Treatment

Use(s)

INDICATIONS & USAGE SECTION

  • For the treatment of acne.
  • Penetrates pores to clear most acne blemishes, acne pimples, blackheads, or whiteheads.

Warning(s)

WARNINGS SECTION

For external use only.

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.

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.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Use every morning and evening
  • Wet area first.
  • Apply a dime sized amount to palm and create a lather.
  • Gently massage over the face and neck.
  • Rinse well.
  • May also be used on chest and back.
  • Because excessive drying of the skin may occur, start with one application daily, 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 swallowed, get medical help or contact a Poison Control Center right away.

Other information

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acetic Acid, Acetyl Hexapeptide-8, Acrylates Copolymer, Allantoin, Aloe Barbadensis Leaf Juice, Arctostaphylos Uva-Ursi Leaf Extract, Aristotelia Leaf Juice, Aristotelia Chilensis Fruit Extract, Ascorbic Acid, Butylene Glycol, Camellia Oleifera Leaf Extract, Citric Acid, Cocamidopropyl Betaine, Dipeptide-2, Euterpe Oleracea Fruit Extract, Fucus Vesiculosus Extract, Glycerin, Glyceryl Caprylate, Glyceryl Undecylenate, Glycolic Acid, Helianthus Annuus (Sunflower) Seed Oil, Hesperidin Methyl Chalcone, Lactic Acid, Lycium Barbarum Fruit Extract, Medicago Sativa (Alfalfa) Extract, Palmitoyl Tetrapeptide-7, Persea Gratissima (Avocado) Oil, Phenoxyethanol, Potassium Sorbate, Prunus Armeniaca (Apricot) Seed Powder, Punica Granatum Fruit Extract, Rubus Idaeus (Raspberry) Fruit Extract, Saccharide Isomerate, Sodium C14-16 Olefin Sulfonate, Sodium Citrate, Sodium Hyaluronate, Sodium Hydroxide, Steareth-20, Tocopheryl Acetate, Water (Aqua)

Questions?

OTC - QUESTIONS SECTION

(888) 322-2612

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label - Carton0Label - Carton0Label - Bottle0Label - Bottle0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038982salicylic acid 1 % Medicated Liquid SoapPSN1
1038982salicylic acid 10 MG/ML Medicated Liquid SoapSCD1
1038982salicylic acid 1 % Medicated Liquid SoapSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73670-606-00NAELI Exfoliator AHA-BHA Face Cleanser177 mL in 1 BOTTLEGEL1771
73670-606-00NAELI Exfoliator AHA-BHA Face Cleanser1 in 1 BOXGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73670-606NAELI EXFOLIATOR AHA-BHA FACE CLEANSER (SALICYLIC ACID) GEL [ALLI LLC]1Current NDC, 2 package rows20250523_16bf50c6-4a9d-4242-94a2-d2165b82e7ce.zip

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73670-60673670-606-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

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
NAELI Exfoliator AHA-BHA Face CleanserSALICYLIC ACIDALLI LLC16bf50c6-4a9d-4242-94a2-d2165b82e7ce2025-05-22WarningsExact identifier
ndc (package): 73670-606-00
ndc (product): 73670-606
ndc11 (package): 73670060600
spl id: 35b6571b-130f-cf57-e063-6294a90aae80
spl set id: 16bf50c6-4a9d-4242-94a2-d2165b82e7ce

Reported adverse events (FAERS/openFDA)#

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