SOME BY MI AHA BHA PHA 30 DAYS MIRACLE TONER

Manufacturer
PERENNEBELL Co., Ltd. | reBom Co., Ltd.
Effective date
2023-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:24:47

Label at a glance#

ProductSOME BY MI AHA BHA PHA 30 DAYS MIRACLE TONER
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.01%

OTC - PURPOSE SECTION

Acne Treatment

INDICATIONS & USAGE SECTION

For the treatment of Acne

DOSAGE & ADMINISTRATION SECTION

Take an appropriate amount and spread evenly onto the skin.

WARNINGS SECTION

For external use only
When using this product, 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. avoid contact with eyes. If contact occurs, flush thoroughly with water.
People with allergy to aspirin will react poorly to the Salicylic Acid.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Dipropylene Glycol, Glycerin, Niacinamide, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Polyglyceryl-4 Caprate, Carica Papaya (Papaya) Fruit Extract, Lens Esculenta (Lentil) Seed Extract, Hamamelis Virginiana (Witch Hazel) Extract, Nelumbo Nucifera Flower Extract, Swiftlet Nest Extract, Sodium Hyaluronate, Fructan, Allantoin, Adenosine, Hydroxyethyl Urea, Xylitol, Lactobionic Acid, Citric Acid, Sodium Citrate, 1,2-Hexanediol, Benzyl Glycol, Ethylhexylglycerin, Raspberry Ketone, Mentha Piperita (Peppermint) Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74472-00374472-003-01, 74472-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
0736d961-8de3-5513-e063-6394a90ae10e6e27c88a-2a5f-4843-9e5e-057d84963a6b2023-10-08WarningsExact identifier
spl id: 0736d961-8de3-5513-e063-6394a90ae10e
spl set id: 6e27c88a-2a5f-4843-9e5e-057d84963a6b

Reported adverse events (FAERS/openFDA)#

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