EQUATE ZIINC SUNSCREEN ULTRA BROAD SPECTRUM- octinoxate, titanium dioxide, zinc oxide cream

Equate ZIinc Sunscreen ULTRA Broad Spectrum by

Drug Labeling and Warnings

Equate ZIinc Sunscreen ULTRA Broad Spectrum by is a Otc medication manufactured, distributed, or labeled by Walmart Stores Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Octinoxate 4.0%

Titanium Dioxide 5.0%

Zinc Oxide 9.1%

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 caused by the sun

Warnings

For external use only

Do not use on damaged 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

reapply:

   after 80 minutes of swimming or sweating

    immediately after towel drying

    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 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-sleeve shirts, pants, hats, and sunglasses

Other information

protect this product from excessive heat and direct sun

may stain or damage some fabrics/materials or surfaces

Inactiveingredients

water, C12-15 alkyl benzoate, cetyl dimethicone, cetyl PEG/PPG-10/1 dimethicone, caprylic/capric triglyceride, ethylhexyl palmitate, tridecyl salicylate, polyethylene, tetradecane, hydrogenated castor oil, hydrogenated polydecene, aloe barbadensis leaf juice, butylene glycol, ethylhexyl stearate, cyclopentasiloxane, cyclohexsiloxane, caprylyl glycol, phenoxyethanol, hydroxyethylcellulose, tetrahexyldecyl ascorbate, triethoxycaprylylsilane, hexylene glycol, dimethicone, tocopheryl acetate, camellia sinensis (green tea) leaf extract, sodium chloride

Satisfaction guaranteed -

For questions or comments please call 1-888-287-1915. 

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE ZIINC SUNSCREEN ULTRA BROAD SPECTRUM 
octinoxate, titanium dioxide, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-564
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	40 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	50 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	91 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
TETRADECANE (UNII: 03LY784Y58)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
DIMETHICONE (UNII: 92RU3N3Y1O)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-564-43	1 in 1 PACKAGE	02/20/2019
1	NDC: 49035-564-42	29.6 mL in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	02/20/2019

Labeler - Walmart Stores Inc. (051957769)

Registrant - Fruit of the Earth Inc. (080086802)

Establishment
Name	Address	ID/FEI	Business Operations
Fruit of the Earth Inc.		079559467	manufacture(49035-564)