Natural Defense Multicolor Stick

Natural Defense Multicolor Stick by

Drug Labeling and Warnings

Natural Defense Multicolor Stick by is a Otc medication manufactured, distributed, or labeled by Physicians Formula, Baja Fur, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NATURAL DEFENSE MULTICOLOR STICK- titanium dioxide, zinc oxide stick 
Physicians Formula

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Natural Defense Multicolor Stick

Active Ingredients

Titanium Dioxide 11%

Zinc Oxide 1.9%

Purpose

Sunscreen

Uses

helps prevent sunburn

If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging cause by the sun

Warnings

For external use only

Do not use on damage or broken skin

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

Stop use 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

apply liberally 15 minutes before sun exposure

use a water resistant sunscreen if swimming or sweating
reapply at least every 2 hours
children under 6 months of age: 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

Other information

Protect this product from excessive heat and direct sun

Inactive Ingredients

Triethylhexanoin, Caprylic/Capric Triglyceride, Dimethicone, Polyethylene, C12-15 Alkyl Benzoate, Silica, Polymethyl Metacrylate, Microcrystalline Wax/Cire Microcristalline, VP/Hexadecene Copolymer, Butyrospermum Parkii (Shea) Butter, Calcium Aluminum Borosilicate, Silica Dimethyl Silylate, HDI/Trimethylol Hexyllactone Crosspolymer, Fragrance/Parfum, Brassica Campestris/Aleurites Fordi Oil Copolymer, Tocopheryl Acetate, Castor Oil Phosphate, Phenoxyethanol, Triethoxycaprylylsilane, Methicone, BHT, Ascorbyl Palmitate, Water/Eau, Lecithin, Plankton Extract. May Contain/Peut Contenir: Carmine (CI 75470), Iron Oxides (CI 77491, CI 77492, CI 77499), Manganese Violet (CI 77742), Mica, Yellow 5 Lake (CI 19140)

Questions or comments?

call 1-800-227-0333 (USA only) or www.PhysiciansFormula.com

Package Label

NATURAL DEFENSE MULTICOLOR STICK 
titanium dioxide, zinc oxide stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 31645-217
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1.9 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	11 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
DIMETHICONE 100 (UNII: RO266O364U)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
CASTOR OIL PHOSPHATE (UNII: SBR4NJI3UJ)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
METHICONE (20 CST) (UNII: 6777U11MKT)
WATER (UNII: 059QF0KO0R)
MICA (UNII: V8A1AW0880)
MANGANESE VIOLET (UNII: 72M48QQV8Q)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
LOW DENSITY POLYETHYLENE (UNII: J245LN42AI)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
SHEA BUTTER (UNII: K49155WL9Y)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CARMINIC ACID (UNII: CID8Z8N95N)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 31645-217-02	1 in 1 CARTON	01/01/2021	12/01/2023
1	NDC: 31645-217-01	7.4 g in 1 CONTAINER; 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	01/01/2021	12/01/2023

Labeler - Physicians Formula (021261805)

Establishment
Name	Address	ID/FEI	Business Operations
Baja Fur, S.A. de C.V.		821533098	manufacture(31645-217) , label(31645-217) , pack(31645-217)

Revised: 12/2023

Document Id: 0d9a2510-81ba-6dfe-e063-6294a90acafc

34390-5

Set id: e5feec09-73ba-e4c0-e053-2995a90a3025

Version: 2

Effective Time: 20231228