NDC | 37000-275-56 |
Set ID | 7cbbc726-7d29-41cf-b70e-d118cbc7be40 |
Category | HUMAN OTC DRUG LABEL |
Packager | The Procter & Gamble Manufacturing Company |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
-
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
-
Directions
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use 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 sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- children under 6 months: ask a doctor
- Other information
-
Inactive ingredients
water, glycerin, isopropyl palmitate, isohexadecane, tocopheryl acetate, aloe barbadensis leaf extract, steareth-21, stearyl alcohol, cetyl alcohol, behenyl alcohol, dimethicone, polyacrylamide, C13-14 isoparaffin, DMDM hydantoin, steareth-2, disodium EDTA, dimethiconol, laureth-7, triethoxycaprylylsilane, oleth-3 phosphate, iodopropynyl butylcarbamate.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 56 g Jar Carton
-
INGREDIENTS AND APPEARANCE
OLAY COMPLETE ALL DAY MOISTURE SENSITIVE WITH BROAD SPECTRUM SPF 15
octinoxate and zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-275 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 6 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 3 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ISOHEXADECANE (UNII: 918X1OUF1E) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) STEARETH-21 (UNII: 53J3F32P58) DOCOSANOL (UNII: 9G1OE216XY) CETYL ALCOHOL (UNII: 936JST6JCN) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) DIMETHICONE (UNII: 92RU3N3Y1O) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) DMDM HYDANTOIN (UNII: BYR0546TOW) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) EDETATE DISODIUM (UNII: 7FLD91C86K) STEARETH-2 (UNII: V56DFE46J5) ALOE VERA LEAF (UNII: ZY81Z83H0X) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) POLYQUATERNIUM-5 (UNII: Q44R132386) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-275-56 1 in 1 CARTON 04/01/2012 1 56 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 not final part352 04/01/2012 Labeler - The Procter & Gamble Manufacturing Company (004238200)