Kiehls Since 1851 Super Multi Corrective Broad Spectrum SPF 30 Sunscreen: Package Insert and Label Information

KIEHLS SINCE 1851 SUPER MULTI CORRECTIVE BROAD SPECTRUM SPF 30 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene cream
L’Oreal USA Products 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.

Active ingredient

Avobenzone 3%

Homosalate 5%

Octisalate 5%

Octocrylene 7%

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

For sunscreen use:

  • 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-sleeved shirts, pants, hats, and sunglasses

  • children under 6 months of age: Ask a doctor

Other information

protect the product in this container from excessive heat and direct sun

Inactive ingredients

water, glycerin, dimethicone, glyceryl stearate, hydroxypropyl tetrahydropyrantriol, silica, PEG-100 stearate, propylene glycol, euphorbia cerifera (candelilla) wax, phenoxyethanol, ammonium polyacryloyldimethyl taurate, stearic acid, dicaprylyl carbonate, cetyl alcohol, palmitic acid, capryloyl salicylic acid, caprylyl glycol, xanthan gum, dimethicone/vinyl dimethicone crosspolymer, fragrance, disodium EDTA, tocopherol, sodium hyaluronate, adenosine, linalool, sodium hydroxide, jasminum officinale (jasmine) flower extract, citronellol, geraniol, citral, benzyl alcohol, citric acid

Questions or comments?

Call toll free 1-800-946-4453

Monday — Friday (9 a.m. to 5 p.m. EST)

image of a label
(click image for full-size original)

image of a label
(click image for full-size original)
image of a label
(click image for full-size original)

KIEHLS SINCE 1851 SUPER MULTI CORRECTIVE BROAD SPECTRUM SPF 30 SUNSCREEN
avobenzone, homosalate, octisalate and octocrylene cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-410
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVOBENZONE (AVOBENZONE) AVOBENZONE 30 mg in 1 mL
HOMOSALATE (HOMOSALATE) HOMOSALATE 50 mg in 1 mL
OCTISALATE (OCTISALATE) OCTISALATE 50 mg in 1 mL
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE 70 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
DIMETHICONE
GLYCERYL MONOSTEARATE
HYDROXYPROPYL TETRAHYDROPYRANTRIOL
SILICON DIOXIDE
PEG-100 STEARATE
PROPYLENE GLYCOL
CANDELILLA WAX
PHENOXYETHANOL
STEARIC ACID
DICAPRYLYL CARBONATE
CETYL ALCOHOL
PALMITIC ACID
CAPRYLOYL SALICYLIC ACID
CAPRYLYL GLYCOL
XANTHAN GUM
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)
EDETATE DISODIUM ANHYDROUS
TOCOPHEROL
HYALURONATE SODIUM
ADENOSINE
LINALOOL, (+/-)-
SODIUM HYDROXIDE
JASMINUM OFFICINALE FLOWER
.BETA.-CITRONELLOL, (+/-)-
GERANIOL
CITRAL
BENZYL ALCOHOL
CITRIC ACID MONOHYDRATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49967-410-01 50 mL in 1 JAR None
2 NDC:49967-410-02 125 mL in 1 JAR None
3 NDC:49967-410-03 75 mL in 1 JAR None
4 NDC:49967-410-04 3 mL in 1 PACKET None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part352 07/01/2015
Labeler — L’Oreal USA Products Inc (002136794)
Establishment
Name Address ID/FEI Operations
L’Oreal USA, Inc. 185931458 manufacture (49967-410)

Revised: 01/2020 L’Oreal USA Products Inc

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2020. All Rights Reserved.