Label: OI LIN NATURAL EMULSION SPF 30- sunscreen, titanium dioxide emulsion
- NDC Code(s): 62191-801-06
- Packager: Sunrider Manufacturing L.P.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 21, 2024
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- PURPOSE
-
INDICATIONS & USAGE
Directions:
- Apply liberally 15 minutes before sun exposure.
reapply:
after 40 minutes of swimming or swatingImmediately 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 againg. 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, expecially from 10 a.m. - 2 p.m.
wear long-sleeve shirts, pants, hats, and sunglasses
Children under 6 months: Ask a doctor - ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
OTHER INGREDIENTS:
Water (Deionized)
Caprylic/Capric Triglyceride
Glycerin
Jojoba Esters
Helianthus Annuus (Sunflower) Seed Oil
Prunus Amygdalus Dulcis (Sweet Almond) Oil
VP/Eicosene Copolymer
Sorbitan Palmitate
Cyclopentasiloxane
Citrus Aurantium Dulcis (Orange) Peel WaxOctyldodecyl Neopentanoate
Polysorbate 60
Sorbitan StearateHydrogen Dimethicone
Alumina
Cetyl Alcohol
Glyceryl StearatePEG-100 Stearate
Dimethiconol
Retinyl Palmitate
Tocopheryl Acetate
Oryzanol
Bisabolol
Stearyl Glycyrrhetinate
Persea Gratissima (Avocado) Oil
TocopherolSaccharide Hydrolysate
Magnesium Aspartate
Biotin
Glycine
Alanine
Urea
Hypericum Perforatum Flower/Leaf/Stem Extract
Xanthan Gum
Royal Jelly Extract
Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract
Aloe Barbadensis Leaf Juice (Aloe Vera Gel)
Beeswax
Vitis Vinifera (Grape) Seed Oil
Aesculus Hippocastanum (Horse Chestnut) Seed Extract
PhenoxyethanolEthylhexylglycerin
Citric Acid
Trisodium EDTAPotassium Sorbate
Triethoxycaprylylsilane
Polyhydroxystearic Acid
Zinc OxideFragrance
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
OI LIN NATURAL EMULSION SPF 30
sunscreen, titanium dioxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62191-801 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.65 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62) HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI) PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL (UNII: 66YXD4DKO9) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) SORBITAN PALMITATE (UNII: 77K6Z421KU) CYCLOPENTASILOXANE (UNII: 0THT5PCI0R) CITRUS AURANTIUM DULCIS (ORANGE) PEEL WAX (UNII: 0U715N387C) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) POLYSORBATE 60 (UNII: CAL22UVI4M) SORBITAN STEARATE (UNII: NVZ4I0H58X) HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N) ALUMINA (UNII: LMI26O6933) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL STEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) DIMETHICONOL (40 CST) (UNII: 343C7U75XW) RETINYL PALMITATE (UNII: 1D1K0N0VVC) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ORYZANOL (UNII: SST9XCL51M) .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC) STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P) PERSEA GRATISSIMA (AVOCADO) OIL (UNII: 6VNO72PFC1) TOCOPHEROL (UNII: R0ZB2556P8) SACCHARIDE ISOMERATE (UNII: W8K377W98I) MAGNESIUM ASPARTATE (UNII: R17X820ROL) BIOTIN (UNII: 6SO6U10H04) GLYCINE (UNII: TE7660XO1C) ALANINE (UNII: OF5P57N2ZX) UREA (UNII: 8W8T17847W) HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) XANTHAN GUM (UNII: TTV12P4NEE) ROYAL JELLY (UNII: L497I37F0C) HAMAMELIS VIRGINIANA WHOLE (UNII: V663Q8TEFU) ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X) BEESWAX (UNII: 2ZA36H0S2V) VITIS VINIFERA (GRAPE) SEED OIL (UNII: 930MLC8XGG) AESCULUS HIPPOCASTANUM SEED OIL (UNII: E0M52HIR1Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CITRIC ACID (UNII: 2968PHW8QP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) TRISODIUM EDTA (UNII: 420IP921MB) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ZINC OXIDE (UNII: SOI2LOH54Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62191-801-06 1 in 1 BOX 10/02/2017 1 71 g 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 Drug part352 10/02/2017 Labeler - Sunrider Manufacturing L.P. (786951475) Registrant - Sunrider Manufacturing L.P. (786951475) Establishment Name Address ID/FEI Business Operations Sunrider Manufacturing L.P. 786951475 manufacture(62191-801)