NDC | 49967-821-01 |
Set ID | ebb529e9-a258-4bef-9518-43ee5b07f33e |
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.
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Directions
For sunscreen use:
● apply liberally 15 minutes before sun exposure
● reapply:
● after 80 minutes of swimming or sweating
● immediately after towel drying
● at least every 2 hours
● 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
synthetic beeswax, isodecyl neopentanoate, C10-18 triglycerides, hydrogenated castor oil, euphorbia cerifera (candelilla) wax, isopropyl palmitate, caprylic/capric triglyceride, squalane, isopropyl myristate, isodecyl salicylate, ozokerite, sorbitan isostearate, stearalkonium hectorite, PEG-5, pentaerythrityl ether, PPG-5 pentaerythrityl ether, polyisobutene, propylene carbonate, glycine soja (soybean) sterols, tocopheryl acetate
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 CROSSTERRAIN UV SKIN PROTECTOR BROAD SPECTRUM SPF 50 SUNSCREEN WATER RESISTANT 80 MINUTES
avobenzone, homosalate, octisalate, octocrylene and oxybenzone ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-821 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 30 mg in 1 g Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate 100 min in 1 g Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 50 mg in 1 g Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 75 mg in 1 g Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 50 mg in 1 g Inactive Ingredients Ingredient Name Strength SYNTHETIC WAX (2900 MW) (UNII: U5UP035C8A) ISODECYL NEOPENTANOATE (UNII: W60VYE24XC) C10-18 TRIGLYCERIDES (UNII: 43AGM4PHPI) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) SQUALANE (UNII: GW89575KF9) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ISODECYL SALICYLATE (UNII: S7097PFP4C) CERESIN (UNII: Q1LS2UJO3A) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) STEARALKONIUM HECTORITE (UNII: OLX698AH5P) POLYETHYLENE GLYCOL 250 (UNII: 5246R0812J) POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52) PROPYLENE CARBONATE (UNII: 8D08K3S51E) SOY STEROL (UNII: PL360EPO9J) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-821-01 40 g in 1 JAR; Type 0: Not a Combination Product 06/01/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 06/01/2010 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA Products Inc 185931458 manufacture(49967-821)