NDC | 31645-189-01, 31645-189-47 |
Set ID | 29c87036-c92f-7066-e054-00144ff88e88 |
Category | HUMAN OTC DRUG LABEL |
Packager | Physicians Formula Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active ingredients
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children
-
Directions
▪ Apply liberally 15 minutes before sun exposure
▪ Use a water resistant sunscreen if swimming or sweating ▪ Reapply:
▪ 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 of 15 or higher and other sun protection measures
including: ▪ Limit time in sun, especially from 10 a.m.- 2 p.m.
▪ Wear long-sleeve shirts, pants, hats, and sunglasses ▪ Children under
6 months: Ask a doctor
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Inactive Ingredients
Ethylhexyl Palmitate, Silica, Caprylic/Capric, Triglyceride, Triisotridecyl Trimellitate, C12-15 Alkyl Benzoate, Hydrogenated Microcrystalline Wax, HDI/Trimethylol Hexyllactone Crosspolymer, Aluminum Starch Octenylsuccinate, Polyethylene,Ozokerite, Synthetic Wax, Hydroxycapric Acid, Hydroxycaprylic Acid, Hydroxycinnamic Acid, Teprenone, Butylene Glycol, Dimethicone, Hydrogen Dimethicone, Kaolin, Mica, PEG-4, Synthetic Fluorphlogopite, Tin Oxide, Phenxoyethanol. May Contain: Blue 1 Lake, Iron Oxides, Red 40 Lake, Titanium Dioxide, Yellow 5 Lake
- Other information
- Questions or Comments?
- Package Label
-
INGREDIENTS AND APPEARANCE
SUPER CC COLOR CORRECTION CARE PRIMER STICK SPF 30
octinoxate, octocrylene, oxybenzone,titanium dioxide, zinc oxide stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:31645-189 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 5.1 g in 100 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 4 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4.2 g in 100 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5.6 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 5.2 g in 100 g Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) PHENOXYETHANOL (UNII: HIE492ZZ3T) STANNIC OXIDE (UNII: KM7N50LOS6) ETHYLHEXYL PALMITATE (UNII: 2865993309) HYDRATED SILICA (UNII: Y6O7T4G8P9) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) TRIISODECYL TRIMELLITATE (UNII: 6IFP38QKFS) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) LOW DENSITY POLYETHYLENE (UNII: J245LN42AI) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) HYDROXYCAPRIC ACID (UNII: B41993WR8W) HYDROXYCAPRYLIC ACID (UNII: 0R6X0G0S8A) P-COUMARIC ACID (UNII: IBS9D1EU3J) TEPRENONE (UNII: S8S8451A4O) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) DIMETHICONE 20 (UNII: H8YMB5QY0D) KAOLIN (UNII: 24H4NWX5CO) MICA (UNII: V8A1AW0880) POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:31645-189-01 1 in 1 BOX 01/15/2016 1 NDC:31645-189-47 13.5 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 01/15/2016 Labeler - Physicians Formula Inc (021261805)