NDC | 49967-027-01 |
Set ID | aca3e919-1bc1-494a-9b8d-b0583da428ea |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
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
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Inactive ingredients
water, glycerin, dimethicone, isopropyl isostearate, PTFE, alcohol denat., dimethicone/vinyl dimethicone crosspolymer, behenyl alcohol, phenoxyethanol, polyacrylamide, fragrance, ammonium acryloldiethyltaurate/steareth-25 methacrylate crosspolymer, disodium stearoyl glutamate, cetyl alcohol, mannitol, PEG-100 stearate, argania spinosa kernel extract, dimethiconol, C13-14 isoparaffin, cetearyl alcohol, methylparaben, tocopheryl acetate, panthenol, arachidyl alcohol, retinyl linoleate, capryloyl salicylic acid, disodium-EDTA, laureth-7, zea mays (corn) starch, carbomer, cetearyl glucoside, sodium cocoyl glutamate, zingiber officinale (ginger) root extract, hydrogenated lecithin, linalool, silica, benzyl salicylate, limonene, hydrolyzed rice protein, benzyl alcohol, methylisothiazolinone, geraniol, citral; may contain: titanium dioxide, iron oxides
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GARNIER ULTRALIFT TRANSFORMER ANTIAGE SKIN CORRECTOR BROAD SPECTRUM SPF 20 SUNSCREEN
octisalate and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-027 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 49 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 44 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-027-01 1 in 1 CARTON 11/15/2013 1 50 mL in 1 TUBE; 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 11/15/2013 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 624244349 manufacture(49967-027)