HARMON FACE VALUES ULTRA LIGHT DRY TO THE TOUCH SUNSCREEN BROAD SPECTRUM SPF 70- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Harmon Face Values Ultra Light Dry to the Touch Sunscreen Broad Spectrum SPF 70 by

Drug Labeling and Warnings

Harmon Face Values Ultra Light Dry to the Touch Sunscreen Broad Spectrum SPF 70 by is a Otc medication manufactured, distributed, or labeled by HARMON STORES, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Avobenzone 3.0%

Homosalate 10.0%

Octisalate 3.0%

Octocrylene 7.0%

Oxybenzone 6.0%

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

• apply liberally 15 minutes before sun exposure

reapply:
after 80 minutes of swimming or sweating
immediately after towel drying
at least every 2 hours

• children under 6 months of age: Ask a doctor

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

Other information

protect the product in this container from excessive heat and direct sun
may stain or damage some fabrics, materials or surfaces

Inactive ingredients

water, styrene/acrylates copolymer, dimethicone, acylates/C12-22 alkyl methacrylate copolymer, propylene glycol, xanthan gum, capryl methicone, polysilicone-15, cetyl dimethicone, glyceryl stearate, PEG-100 stearate, beeswax, silica, dipotassium glycyrrhizate, trimethylsiloxysilicate, sodium polyacrylate, ethylhexyl stearate, trideceth-6, phenoxyethanol, caprylyl glycol, ethylhexylglycerin, disodium EDTA, fragrance

PRINCIPAL DISPLAY PANEL

Harmon Face Values Ultra Light Dry to the Touch Sunscreen Lotion Broad Spectrum SPF 70

6.0 fl oz (177 mL)

NDC: 63940-075-94

INGREDIENTS AND APPEARANCE

HARMON FACE VALUES ULTRA LIGHT DRY TO THE TOUCH SUNSCREEN BROAD SPECTRUM SPF 70 
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63940-075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	70 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	30 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	60 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
EDETATE DISODIUM (UNII: 7FLD91C86K)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
TRIMETHYLSILOXYSILICATE (M/Q 0.8-1.0) (UNII: 25LXE464L2)
XANTHAN GUM (UNII: TTV12P4NEE)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
DIMETHICONE (UNII: 92RU3N3Y1O)
WATER (UNII: 059QF0KO0R)
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
POLYSILICONE-15 (UNII: F8DRP5BB29)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
WHITE WAX (UNII: 7G1J5DA97F)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CETYL DIMETHICONE 45 (UNII: IK315POC44)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63940-075-94	177 mL in 1 TUBE; Type 0: Not a Combination Product	08/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	08/29/2019

Labeler - HARMON STORES, INC. (804085293)