DRS. PHARMACY SUNSCREEN SPF 30- sunscreen spf 30 lotion 
OL PHARMA TECH LLC. (Drs. Pharmacy)

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ACTIVE INGREDIENTS

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 10%

PURPOSE

Sunscreen Agent

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

• May stain some fabrics and surfaces.

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove it

Stop use and ask a doctor

if rash occurs

Keep out of reach of children

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

Inctive ingredients

Water, Carbomer,capric/caprylic Triglyceride, Glycerin, Sodium Hydroxide, Propylene Glycol, Xanthan Gum, methyl glycose sesquistearate,PEG-20 methyl glycose sesquistearate, Cyclomethicone, Behenyl alcohol, Isopropyl isostearate, phenoxyethanol, Methyl Gluceth-20, Disodium EDTA.

other information

protect this product from excessive heat and direct sunlight

Questions

www.drspharmacyusa.com

spf30 lotion

DRS. PHARMACY SUNSCREEN SPF 30 
sunscreen spf 30 lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-232
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE10 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PEG-20 METHYL GLUCOSE SESQUISTEARATE (UNII: 0345752X7U)  
CYCLOMETHICONE (UNII: NMQ347994Z)  
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)  
SODIUM HYDRIDE (UNII: 23J3BHR95O)  
DOCOSANOL (UNII: 9G1OE216XY)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80489-232-01133 g in 1 TUBE; Type 0: Not a Combination Product01/01/2024
2NDC:80489-232-02118 g in 1 TUBE; Type 0: Not a Combination Product01/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/01/2024
Labeler - OL PHARMA TECH LLC. (Drs. Pharmacy) (021170377)
Registrant - OL PHARMA TECH LLC. (021170377)
Establishment
NameAddressID/FEIBusiness Operations
OL PHARMA TECH LLC., (Drs. Pharmacy)021170377manufacture(80489-232)

Revised: 1/2024
Document Id: 0def1454-0c3f-5a66-e063-6294a90ae1b7
Set id: 052dea5d-a775-8dc2-e063-6294a90a4f19
Version: 2
Effective Time: 20240101
 
OL PHARMA TECH LLC. (Drs. Pharmacy)