ID ANTI-ACNE OIL FREE LOTION

Manufacturer
SKIN SCIENCES LABORATORY INC. | SKIN PRESCRIPTIVES MARKETING, INC.
Effective date
2017-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:51

Label at a glance#

ProductID ANTI ACNE
Active ingredientSALICYLIC ACID
Label structure10 sections

Storage and handling

Other information - Protect the product in this container from excessive heat and direct sun. - Before use, test a tiny amount on skin (we omit allergens, but you may be sensitive to an ingredient that is not an allergen. - Introduce new skin products one at a time, with at least 3 days in between. - Do not (re)introduce removed portions of product or other substances into container.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Salicylic Acid 1.95%

OTC - PURPOSE SECTION

Purpose

Acne Treatment

INDICATIONS & USAGE SECTION

Uses

Treats acne • Helps prevent development of new acne blemishes

WARNINGS SECTION

Warnings

For external use only

When using lhis product

• Apply to affected areas only

• Avoid unnecessary sun exposure and use a sunscreen

• Do not use in or near the eyes.

Using other topical acne drugs at the same time

or right after use of this product
may increase dryness or irritation of the skin.
Only one drug should be used unless directed by a doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep oul of reach of children, if swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

• Clean Directions skin well before applying this product

• Dot and spread gently over face, neck, chest, back, back of arms, thighs, posterior and other affected areas. Avoid mucosaI (wet) areas of eyes, nostrils and mouth.
• Follow with a sunscreen.
• Because excessive drying of the skin may occur, start applying 2x-a-week only, very slowly increasing until 2x-a-day usage is achieved (no earlier than week 8). Do not rush.

If bothersome dryness or peeling occurs, stop for 5-7 days and restart application frequency at 2x-a-week, slowly increasing over several weeks.

STORAGE AND HANDLING SECTION

Other information
- Protect the product in this container from excessive heat and direct sun.
- Before use, test a tiny amount on skin (we omit allergens, but you may be sensitive
to an ingredient that is not an allergen.
- Introduce new skin products one at a time, with at least 3 days in between.
- Do not (re)introduce removed portions of product or other substances into container.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Alcohol, Inactive Aq !:J,redients ater/Eau, Butylene Glycol, C12-15 Alkyl Lactate, Camellia Sinensis Leaf ElCl:ract, Ceteareth-25, Getearyl Alcohol, Gyclol)entasilox- ane, Glycerin, Glyceryl Caprate, Glyceryl Laurate, Glyceryl Stearate, Sodium Phytate, Tromethamine.

OTHER SAFETY INFORMATION

Notes: If contact with eyes
occurs, flush out with plenty of
water. This product is meant to be washed off quickly, not left on the
skin for longer than a few seconds
while cleansing. Prolonged
exposure without rinsing
immediately may cause irritation to
skin. Stop use and consult your
doctor in the unlikely event of
discomfort or sensitivity. 1ST-TIME
USERS: Some first-time users may
experience an initial acne
break-out due to the deeper
exfoliation of the pores' inner
walls. If your pores have not been
regularly cleaned at this level,
existing pore cloggers are brought
to the surface. As therapy
continues, this deeper-cleaned
state is maintained and acne is
markedly reduced. With correct
use - following instructions
carefully, the slow increase in
application frequency, the use of
hypoallergenic, non-comedogenic
and pH-appropriate support
products in the Id system - as well
as prevention with non-comedo-
genic products such as Essence
Skin-Saving Hair, Body + Bath Care,
Armada Sun + Light Screens,
Skintelligent Beauty Makeup, this
initial reaction soon disappears. If it
does occur, stop use for 1 week
and restart therapy at the
beginning, with 2x-a-week
applications. CYSTIC ACNE can
be internally caused. If you have
cystic acne, consult your
dermatologist as you may need
additional medication and/or other
management.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

VMV HYPOALLERGENICS
validated hypoallergenic.
randomized, blinded, published &
awarded clinical studies. since 1979

id
OIL-FREE
CLARIFYING LOTION

face + body anti-acne
exfoliating hydrator

salicylic acid+ monolaurin: glycerin; antioxidants: green tea+ rice phytic acid
clarifying, smoothening+ exfoliating system

Validated
Hypoallergenic:
VH -109/109
sans all common allergens,
extended allergen series:
North American Contact Dermatitis
Group + European Surveillance
System on Contact Allergies

100% All-Types-Of-Fragrance-Free.

100% Dye, Phthalate, Paraben + Preservative-Free.

Usage, Patch + Clinically-Tested (in vitro + in vivo; evidence-based:
double-blind, randomized).

Non-Comedogenic. Non-Drying.

For All Skin Types.

For Men + Women, 18+.

110 mL (3.72 Fl. Oz.) - 110 mL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69774-553-042020-01-31C16284748780-19d75b9cf-fe69-f424-e053-dadaa90a57ceID ANTI-ACNE OIL FREE LOTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69774-553-04ID ANTI ACNE110 mL in 1 BOTTLE, PUMPLOTION1101
69774-553-04ID ANTI ACNE1 in 1 BOXLOTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69774-553ID ANTI ACNE (SALICYLIC ACID) LOTION [SKIN SCIENCES LABORATORY INC.]1Legacy NDC, 2 package rows20170513_4ddf653c-2e00-28bd-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69774-55369774-553-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
4ddf653c-2e01-28bd-e054-00144ff8d46c4ddf653c-2e00-28bd-e054-00144ff8d46c2017-04-23WarningsExact identifier
spl id: 4ddf653c-2e01-28bd-e054-00144ff8d46c
spl set id: 4ddf653c-2e00-28bd-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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