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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

PanOxyl Oil Control Moisturizer with SPF 30 Mineral Sunscreen

Active Ingredients

Titanium Dioxide - 1.0%

Zinc Oxide - 7.8%

Purpose

Sunscreen

Uses

Warnings

• When using this product • Keep out of eyes. Rinse with water to remove

• Stop use and ask doctor if rash or irritation occurs

Do not use: • On damaged or broken skin • If allergic to any ingredient

• If swallowed, get medical help or contact a Poison Control Center

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

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 Daily Moisturizer

Absorbs Excess Oil

UVA/UVB Protection

Won't Clog Pores

P11833.00

panoxyloilcontrolam

PanOxyl Oil Control Moisturizer 1.7oz Carton

New

DERMATOLOGIST RECOMMENDED

PanOxyl AM

OIL CONTROL MOISTURIZER

Broad Spectrum SPF 30

Mineral Sunscreen

Lightweight Daily Moisturizer

Absorbs Excess Oil

UVA/UVB Protection

Won't Clog Pores

P11834.01

panoxylocmcarton

PANOXYL OIL CONTROL MOISTURIZER 
titanium dioxide and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0263
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE10 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE83.4 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0263-021 in 1 CARTON03/09/2021
148 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/09/2021
Labeler - Crown Laboratories (079035945)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories079035945manufacture(0316-0263)

Revised: 2/2023
Document Id: f49cf15f-5539-6fbd-e053-2a95a90a6bd8
Set id: bd31b4eb-b419-19c3-e053-2995a90ae757
Version: 3
Effective Time: 20230213
 
Crown Laboratories