FDA.reportPublic FDA data

AcNesic Acne Treatment

Manufacturer
Blaine Labs Inc.
Effective date
2021-04-29
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:45:36

Label at a glance#

ProductAcNesic Acne Treatment
Active ingredientSALICYLIC ACID
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION

Wash the affected skin with soap and water. Allow to dry
thoroughly. Apply a thin layer 1-3 times per day.

INDICATIONS & USAGE SECTION

INDICATIONS AND USAGE

Indicated for the treatment of acne. Clears and prevents
acne pimples, blackheads, whiteheads and acne blemishes.

For external usage only. Avoid contact with eyes.

WARNINGS SECTION

KEEP OUT OF REACH OF CHILDREN.

OTHER SAFETY INFORMATION

Store at room temperature 20°C-25°C (68°F-77°F).
For complete prescribing information, see package insert.

HOW SUPPLIED SECTION

ACTIVE INGREDIENT
Salycilic Acid 0.5% (Acne Treatment).

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS
Aloe barbadensis leaf extract, benzalkonium chloride,
butylene glycol, butylparaben, carbomer, deionized water,
ethylparaben, glycerin, hyaluronic acid, hydrolyzed egg shell
membrane, isobutylparaben, methylparaben,
phenoxyethanol, polysorbate 20, propylene glycol,
propylparaben, triethanolamine.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 63347-920-01

BLAINE LABS®​

AcNesic®​

ACNE TREATMENT

(SALICYLIC ACID 0.5%)

FOR TOPICAL USE ONLY

RX ONLY

1.7 OZ (48 g)

QUESTIONS OR COMMENTS?
800.307.8818 | BlaineLabs.com
M-F, 7:30 am - 3:30 pm (PST)
Contact@BlaineLabs.com

MANUFACTURED BY:
Blaine Labs, Inc.
11037 Lockport Place
Santa Fe Springs, CA 90670

25100-P-LBL01          REV20210409

Box

920 Box920 Box

Bottle

920 Botl920 Botl

Insert

920 Insert920 Insert

res

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63347-920-01GM - Gram63347-9205709ea5b-2832-4c96-9ca1-f7c02fec280712021-06-02

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63347-92063347-920-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
ALOE VERA LEAFZY81Z83H0XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
BUTYLPARABEN3QPI1U3FV8IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ETHYLPARABEN14255EXE39IACT
GLYCERINPDC6A3C0OXIACT
HYALURONIC ACIDS270N0TRQYIACT
EGG SHELL MEMBRANEN7QBR4212VIACT
ISOBUTYLPARABEN0QQJ25X58GIACT
METHYLPARABENA2I8C7HI9TIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PROPYLPARABENZ8IX2SC1OHIACT
TROLAMINE9O3K93S3TKIACT

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
20da8eb4-bb1d-44de-b657-8edfce4fcd81bc72f728-7cd0-46c3-9d70-55223b097cd22022-12-12WarningsExact identifier
spl set id: bc72f728-7cd0-46c3-9d70-55223b097cd2

Reported adverse events (FAERS/openFDA)#

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