RENEWED HOPE IN A JAR SKIN TINT SPF 20- octinoxate, titanium dioxide liquid

renewed hope in a jar skin tint spf 20 by

Drug Labeling and Warnings

renewed hope in a jar skin tint spf 20 by is a Otc medication manufactured, distributed, or labeled by PHILOSOPHY, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Titanium Dioxide (2.6%), Octinoxate (2.0%)

Purpose

Sunscreen

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

For external use only.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

use in the morning as your daily moisturizer

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: [bullet] limit time in the sun, especially from 10 a.m.-2 p.m. [bullet] wear long-sleeved shirts, pants, hats, and sunglasses.
children under 6 months of age: ask a doctor

Inactive Ingredients

Other Information

protect this product in this container from excessive heat and direct sun

Questions or Comments?

Call toll-free 1-800-568-3151 from 9 a.m.-8 p.m. ET (Monday-Friday)

PRINCIPAL DISPLAY PANEL

renewed

hope

in a jar skin tint

philosophy: live with optimism. renew with hope.

whipped water-gel broad spectrum spf 20 sunscreen

skin. color.

INGREDIENTS AND APPEARANCE

RENEWED HOPE IN A JAR SKIN TINT SPF 20 
octinoxate, titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50184-1063
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.6 g  in 100 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
MICA (UNII: V8A1AW0880)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
ALUMINUM DIMYRISTATE (UNII: J2KA067N9O)
SODIUM NITRATE (UNII: 8M4L3H2ZVZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50184-1063-1	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
2	NDC: 50184-1063-2	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
3	NDC: 50184-1063-3	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
4	NDC: 50184-1063-4	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
5	NDC: 50184-1063-5	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
6	NDC: 50184-1063-6	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
7	NDC: 50184-1063-7	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
8	NDC: 50184-1063-8	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019
9	NDC: 50184-1063-9	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/19/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/19/2019

Labeler - PHILOSOPHY, INC. (948102256)