Equitance Sunscreen Broad Spectrum SPF 36 Octinoxate 6.5%Zinc Oxide 16.88%

Equitance Sunscreen Broad Spectrum SPF 36 by

Drug Labeling and Warnings

Equitance Sunscreen Broad Spectrum SPF 36 by is a Otc medication manufactured, distributed, or labeled by Sunstar Americas, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

EQUITANCE SUNSCREEN BROAD SPECTRUM SPF 36- octinoxate zinc oxide lotion 
Sunstar Americas, Inc

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.

----------

Equitance Sunscreen Broad Spectrum SPF 36
Octinoxate 6.5%
Zinc Oxide 16.88%

Drug Facts


Active Ingredients

Octinoxate 6.5%
Zinc Oxide 16.88%

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

Directions

  • apply liberally 15 minutes before sun exposure.
  • reapply at least every 2 hours.
  • use a water resistant sunscreen if swimming or sweating.
  • 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-sleeve shirts, pants, hats and sunglasses.
  • children under 6 months: Ask a doctor.

Other Information

protect this product from excessive heat and direct sun.

Inactive Ingredients

cyclopentasiloxane, water, isotridecyl isononanoate, butylene glycol, silica, methyl methacrylate crosspolymer, peg-20, dimethicone, peg-9 polydimethylsiloxyethyl dimethicone, ascorbyl glucoside, polymethylsilsesquioxane, vinyl dimethicone/methicone silsesquioxane crosspolymer, hydrogen dimethicone, linoleic acid, prunus yedoensis leaf extract, alpinia speciosa leaf extract, aluminum hydroxide, cellulose acetate, citric
acid, dimethicone/vinyl dimethicone crosspolymer, disteardimonium hectorite, fragrance, glycosyl trehalose, hydrogenated starch hydrolysate, magnesium carbonate, mica, phenoxyethanol, sodium chloride, sodium citrate, sodium hyaluronate, sodium hydroxide, sorbitan sesquiisostearate, stearyl glycyrrhetinate, tetrasodium edta, tocopherol.

sunscreen broad spectrum SPF 36

skin brightening broad spectrum protection + make-up primer

discover your path to inner health and radiant beauty. equitance sunscreen broad spectrum protection SPF36 protects and restores skin from visible daily environmental damage. equitance works inside and out to restore and nourish your skin.
grounded in japanese tradition, equitance brightening collection contains japanese herbs as well as clinically proven ingredients developed through 18 years of brightening research. the perfect balance of eastern and western skincare practices, equitance helps you on your journey
towards restored, luminous skin.

USAGE:
SHAKE BOTTLE VERTICALLY UNTIL THE MIXING BALL INSIDE CAN BE HEARD MULTIPLE TIMES, THEN SMOOTH OVER ENTIRE FACE AND NECK AS A FINAL STEP IN YOUR SKIN CARE ROUTINE. REAPPLY AT LEAST EVERY 2 HOURS.

MANUFACTURED FOR:
SUNSTAR AMERICAS, INC.
301 E. CENTRAL RD., SCHAUMBURG,
IL 60195 1-855-827-0362
WWW.EQUITANCE-US.COM
MADE IN JAPAN
DOC02864 R01

Questions?

Call toll free 1-855-827-0362
Mon-Fri ( 9 a.m. - 5 p.m. CST)

Equitance sunscreen broad spectrum protection SPF36
sunscreen
broad spectrum
SPF 36
skin brightening
broad spectrum protection
+ make-up primer
29mL net 0.98 FL. OZ

EQ1

EQ2

EQUITANCE SUNSCREEN BROAD SPECTRUM SPF 36 
octinoxate zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 52376-040
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE6.5 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION16.88 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
WATER (UNII: 059QF0KO0R)  
isotridecyl isononanoate (UNII: WEF51750MT)  
butylene glycol (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
methyl methacrylate (UNII: 196OC77688)  
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)  
dimethicone (UNII: 92RU3N3Y1O)  
POLYETHYLENE GLYCOL 450 (UNII: 5IRA46LB71)  
ascorbyl glucoside (UNII: 2V52R0NHXW)  
POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)  
linoleic acid (UNII: 9KJL21T0QJ)  
PRUNUS X YEDOENSIS LEAF (UNII: 1Z125GA907)  
ALPINIA ZERUMBET LEAF (UNII: MS8P33AMKX)  
aluminum hydroxide (UNII: 5QB0T2IUN0)  
cellulose acetate (UNII: 3J2P07GVB6)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
disteardimonium hectorite (UNII: X687XDK09L)  
TREHALOSE (UNII: B8WCK70T7I)  
STARCH, CORN (UNII: O8232NY3SJ)  
magnesium carbonate (UNII: 0E53J927NA)  
mica (UNII: V8A1AW0880)  
phenoxyethanol (UNII: HIE492ZZ3T)  
sodium chloride (UNII: 451W47IQ8X)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
sodium hydroxide (UNII: 55X04QC32I)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
stearyl glycyrrhetinate (UNII: 3YYE6VJS0P)  
EDETATE SODIUM (UNII: MP1J8420LU)  
tocopherol (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 52376-040-060.6 mL in 1 BOTTLE; Type 0: Not a Combination Product04/12/201612/31/2016
2NDC: 52376-040-0729 mL in 1 BOTTLE; Type 0: Not a Combination Product04/12/201612/31/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35204/12/201612/31/2016
Labeler - Sunstar Americas, Inc (025066358)

Revised: 1/2020
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.