PanOxyl Oil Control Moisturizer with SPF 30 Mineral Sunscreen

PanOxyl Oil Control Moisturizer by

Drug Labeling and Warnings

PanOxyl Oil Control Moisturizer by is a Otc medication manufactured, distributed, or labeled by Crown Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PANOXYL OIL CONTROL MOISTURIZER- titanium dioxide and zinc oxide lotion 
Crown Laboratories

----------

PanOxyl Oil Control Moisturizer with SPF 30 Mineral Sunscreen

Active Ingredients

Titanium Dioxide - 1.0%

Zinc Oxide - 7.8%

Purpose

Sunscreen

Uses

• Helps prevent sunburn and photodamage caused by UVA/UVB exposure
• Higher SPF gives more sunburn protection
• If used as directed with other sun protection measures (see Directions), decreases the risks of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use

• on damaged or broken skin
• if allergic to any ingredient

When using this product

• keep out of eyes. Rinse with water to remove.

Stop and ask a doctor if

• rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Shake well prior to use

Apply liberally to dry skin 15 minutes before sun exposure

For topical use only

Keep out of reach of children Children under 6 months: ask a doctor

Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2 p.m.

Wear long-sleeved shirts, pants, hats, and sunglasses.

Reapply to dry skin: At least every 2 hours Use a water resistant suscreen if swimming for sweating

Other Information

• Protect the product in this container from excessive heat and direct sun
• May stain some fabrics

Inactive Ingredients

Alumina, Aluminum Starch Octenylsucciante, Aluminum Stearate, Beeswax, C12-15 Alkyl Benzoate, C13-14 Isoparaffin, Caffeine, Camellia Sinensis Leaf (Green Tea) Extract, Caprylyl Glycol, Chlorphenesin, Cyclomethicone, Dimethoxydiphenylsilane/Triethoxycaprylylsilane Crosspolymer, Isostearyl Alcohol, Laureth-7, Lauryl PEG/PPG 18/18 Methicone, Phenoxyethanol, Polyacrylamide, Polyhydroxystearic Acid, Purified Water, Sodium Hyaluronate, Triethoxycaprylylsilane

Questions?

Call 800.877.8869

or visit www.panoxyl.com

Crown Laboratories, Inc., Johnson City, TN 37604

Made in USA

PanOxyl Oil Control Moisturizer 1.7oz Tube

DERMATOLOGIST RECOMMENDED

PanOxyl AM

OIL CONTROL MOISTURIZER

Broad Spectrum SPF 30

Mineral Sunscreen

Lightweight Dialy Moisturizer

Absorbs Excess Oil

UVA/UVB Protection

Won't Clog Pores

P11833.00

PANOXYL OIL CONTROL MOISTURIZER 
titanium dioxide and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0316-0263
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	10 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	83.4 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
YELLOW WAX (UNII: 2ZA36H0S2V)
CAFFEINE (UNII: 3G6A5W338E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CHLORPHENESIN (UNII: I670DAL4SZ)
LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
ALUMINUM STEARATE (UNII: U6XF9NP8HM)
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
DIMETHOXYDIPHENYLSILANE (UNII: 02QB6788GC)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ALUMINUM OXIDE (UNII: LMI26O6933)
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
CYCLOMETHICONE (UNII: NMQ347994Z)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
LAURETH-7 (UNII: Z95S6G8201)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0316-0263-02	1 in 1 CARTON	03/09/2021	05/31/2024
1		48 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/09/2021	05/31/2024

Labeler - Crown Laboratories (079035945)

Registrant - Crown Laboratories (079035945)

Revised: 6/2024

Document Id: 1ba7546c-f5b0-6cc8-e063-6394a90a4cd7

34390-5

Set id: bd31b4eb-b419-19c3-e053-2995a90ae757

Version: 4

Effective Time: 20240624