CARDON- avobenzone, homosalate, octyl salicylate lotion

Cardon by

Drug Labeling and Warnings

Cardon by is a Otc medication manufactured, distributed, or labeled by Cardon, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients

Avobenzone 2.5%

Homosalate 7.0%

Octyl salicylate 4.3%

PURPOSE

Purpose

Sunscreen

INDICATIONS & USAGE

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

Warnings

• For external use only

DO NOT USE

• Do not use on damaged or broken skin

WHEN USING

• When using this product keep out of eyes. Rinse with water to remove.

STOP USE

• Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

• Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

• For Sunscreen Use: 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 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-sleeve shirts, pants, hats and sunglasses
• Children under 6 months; Ask a doctor

STORAGE AND HANDLING

Other information

• protect this product from excessive heat and direct sun

STORAGE AND HANDLING

Other information

• protect this product from excessive heat and direct sun

INACTIVE INGREDIENT

Inactive ingredients water, propanediol, butyloctyl salicylate, ethylhexyl methoxycrylene, polymethyl methacrylate, butylene glycol, 1,2-hexanediol, styrene/acrylates copolymer, phenoxyethanol, fragrance, glycerin, pentylene glycol, saccharide hydrolysate, sodium acrylate/sodiumacryloyldimethyl taurate copolymer, carbomer, polyacrylate crosspolymer-6, behenyl alcohol, ethylhexyglycerin, hydroxyethyl acrylate/sodiumacryloyldimethyl taurate copolymer, tromethamine, xanthan gum, isohexadecane, curcuma longa (turmeric) root extract, portulaca oleracea extract, centella asiatica extract, houttuynia cordata extract, salvia hispanica seed extract, opuntia ficus-indica stem extract, t-butyl alcohol, disodium edta, oxygen

SPL UNCLASSIFIED SECTION

Distributed by Cardon LLC, NY, NY 10004 USA

Made in Korea

PRINCIPAL DISPLAY PANEL

CARDON

SPF + MOISTURIZER

BROAD SPECTRUM SPF 30

1.2 FL.OZ. / 35 ml

INGREDIENTS AND APPEARANCE

CARDON 
avobenzone, homosalate, octyl salicylate lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72475-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.3 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
TROMETHAMINE (UNII: 023C2WHX2V)
ISOHEXADECANE (UNII: 918X1OUF1E)
HOUTTUYNIA CORDATA WHOLE (UNII: O3E12ZLW5T)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
DOCOSANOL (UNII: 9G1OE216XY)
XANTHAN GUM (UNII: TTV12P4NEE)
TURMERIC (UNII: 856YO1Z64F)
PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
SALVIA HISPANICA SEED (UNII: NU0OLX06F8)
OPUNTIA FICUS-INDICA STEM (UNII: MUD8892KHL)
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
INVERT SUGAR (UNII: ED959S6ACY)
EDETATE DISODIUM (UNII: 7FLD91C86K)
OXYGEN (UNII: S88TT14065)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72475-001-35	35 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/09/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	08/09/2018

Labeler - Cardon LLC (096323521)