ANTI-EVERYTHING FACE MOISTURIZER- salicylic acid cream lotion

Anti-Everything Face Moisturizer by

Drug Labeling and Warnings

Anti-Everything Face Moisturizer by is a Otc medication manufactured, distributed, or labeled by Bentley Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

Active Ingredients

Salicylic Acid  1.0%

PURPOSE

Purpose

Acne Treatment

INDICATIONS & USAGE

Uses
For the treatment of acne
Reduces the number of acne pimples,
blackheads, whiteheads and allows
skin to heal
Penetrates pores to clear most acne
blemishes
Helps prevent new acne blemishes
from formlng

WARNINGS

Warnings
For external use only

Do not use if you have very sensitive
skin or known allergy to aspirin

Slop use and ask a doctor if
excessive itching, dryness, redness,
burning, or swelling occurs or if these
symptoms persist

When using this product  Keep
away from eyes, lips, and other
mucous membranes. If contact occurs,
flush thoroughly with water. Using
other topical acne medications at the
same time or immediately following
use of this product may increase
dryness or irritation of the skin. If this
occurs, only one medication should be
used unless directed by doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children. If
swallowed get medical help or contact
Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions
Squeeze 1-2 pumps on to fingertips.
Apply evenly on clean, dry skin at
night. Avoid eye area. Suggested use
in PM.
At first, use every other day. Then
up to twice a day as tolerated
Use sunscreen during the day while
using this product
Because excessive drying of the skin
may occur, start with one application
daily, then gradually increase if needed
or as directed by a doctor.
If bothersome dryness or peeling
occurs, reduce the application.
Store dry at room temperature

INACTIVE INGREDIENT

Inactive ingredients Water,
Cetyl Alcohol, Dimethicone,
Caprylic/Capric Triglyceride, Glyceryl
Stearate Citrate, Ammonium
Acryloyldimethyltaurate/VP Copolymer,
Glycolic Acid, Squalane, Dicaprylyl
Carbonate, Glycerin, Phenoxyethanol,
Sodium Hydroxide, Isopentyldiol, Sodium
Stearoyl Glutamate, Polyacrylate
Crosspolymer-6, Dimethicone/Vinyl
Dimethicone Crosspolymer, Cladonia
Stellaris Extract (Alpine Caribou Moss™),
Ethylhexylglycerin, Gluconolactone,
Trifolium Pratense (Clover) Flower Extract,
Sodium Hyaluronate, Arctium Majus
(Burdock) Root Extract, Portulaca
Oleracea Extract, Sodium Benzoate

SPL UNCLASSIFIED SECTION

Other Information Sunburn Alert.
This product contains an alpha hydroxy
acid (AHA) that may increase your skin's
sensitivity to the sun and particularly the
possibility of sunburn. Use a sunscreen,
wear protective clothing, and limit sun
exposure while using this product and
for a week afterwards.

QUESTIONS

Questions or comments?

Email us at HI@oarsandalps.com

Product Packaging: OARS + ALPS ANTI-EVERYTHING FACE MOISTURIZER

OARS + ALPS

ANTI-EVERYTHING

FACE MOISTURIZER

1% SALICYLIC ACID

1.7 Fl. Oz. / 50 mL

Manufactured for

Oars + Alps LLC

Chicago, IL 60661

res 080624

INGREDIENTS AND APPEARANCE

ANTI-EVERYTHING FACE MOISTURIZER 
salicylic acid cream lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-181
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	Salicylic Acid	1.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE (UNII: 92RU3N3Y1O)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
SQUALANE (UNII: GW89575KF9)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ISOPENTYLDIOL (UNII: 19NOL5474Q)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
CLADONIA RANGIFERINA WHOLE (UNII: O21ZF987XQ)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
PORTULACA OLERACEA LEAF (UNII: 9JW9D9JGHZ)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-181-01	1 in 1 CARTON	08/08/2024
1		50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	08/08/2024

Labeler - Bentley Laboratories, LLC (068351753)