HANSON DAILY MOISTURIZER SPF30- octisalate, homosalate, avobenzone, octocrylene lotion 
Hanson Medical, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Hanson Daily Moisturizer Broad Spectrum SPF 30

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

HansonSPF30

HANSON DAILY MOISTURIZER  SPF30
octisalate, homosalate, avobenzone, octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65177-290
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE5 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE2.7 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65177-290-0159.1 mL in 1 TUBE; Type 0: Not a Combination Product10/10/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35210/10/201504/30/2021
Labeler - Hanson Medical, Inc (049119329)

Revised: 6/2021
Document Id: 291f9c1c-f942-4807-8922-bb9e51c286ea
Set id: 35a12458-9495-4676-bb8c-819ad33136d0
Version: 13
Effective Time: 20210619
 
Hanson Medical, Inc