HANSON DAILY MOISTURIZER SPF30- octisalate, homosalate, avobenzone, octocrylene lotion

Hanson Daily Moisturizer by

Drug Labeling and Warnings

Hanson Daily Moisturizer by is a Otc medication manufactured, distributed, or labeled by Hanson Medical, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Octisalate 5.0%

Homosalate 5.0%

Avobenzone 3.0%

Octocrylene 2.7%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If used as directed with other sun protection measures (see ​Directions​), decreased the risk of skin cancer and early skin aging cause by the sun

WARNINGS

For External Use Only

Do not use

on damanged or broken skin

When using this product

keep out of eyes, rinse with water to remove

Stop us and consult a doctor

   if rash occurs

Keep out of reach of children.

If product is swallowed, get medical attention or contact a ​Poison Control Center​ right away.

Directions

• Apply liberally 15 minutes before sun exposure
• Use a water resistant sunscreen if swimming or sweating
• Reapply 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 broad spectrum SPF of 15 or higher and use other sun protection measures including

•    Limit time in the sun, especially from 10am-2pm
•    Wear long sleeve shirts, pants, hats, and sunglasses
• For children under 6 months: Ask a doctor

Inactive Ingredients

Aloe Barbadensis (Aloe Vera) Leaf Juice, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Ammonium Acryloyldimethyltaurate/VP Copolymer,
Butylene Glycol, Caprylyl Glycol, Cetearyl Alcohol, Chlorphenesin, Citrus Sinensis (Blood Orange) Fruit Extract, Coco Caprylate/Caprate, Decyl Glucoside, Dextrin, Dimethicone, Disodium EDTA, Ethylhexyl Stearate, Fragrance, Glycerin, Glyceryl Stearate, Hydrolyzed Hibiscus Esculentus Extract, Isododecane, PEG-100 Stearate, Pentylene Glycol, Phenoxyethanol, Polysilicone-11, Polyurethane-34, Sodium Citrate, Sodium Polyacrylate, Tapioca Starch Polymethylsilsesquioxane, Tocopheryl Acetate, Trideceth 6, Water, Xanthan Gum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANSON DAILY MOISTURIZER  SPF30
octisalate, homosalate, avobenzone, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65177-290
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	5 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.7 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CHLORPHENESIN (UNII: I670DAL4SZ)
CITRUS SINENSIS WHOLE (UNII: 37673443KL)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE SODIUM (UNII: MP1J8420LU)
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ABELMOSCHUS ESCULENTUS SEED (UNII: 1GJ68JL4J5)
ISODODECANE (UNII: A8289P68Y2)
PEG-100 STEARATE (UNII: YD01N1999R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
POLYURETHANE-34 (40 MPA, TENSILE STRENGTH OF FILM AT BREAK) (UNII: 77KA3O6NNF)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
STARCH, TAPIOCA (UNII: 24SC3U704I)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65177-290-01	59.1 mL in 1 TUBE; Type 0: Not a Combination Product	10/10/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	10/10/2015

Labeler - Hanson Medical, Inc (049119329)