DAILY FACIAL MOISTURIZER SPF 35- octinoxate and avobenzone lotion 
Pharmco Laboratories Inc.

----------

Daily Facial Moisturizer SPF 35

Drug Facts

Active Ingredient:Purpose
Avobenzone 2.5%Sunscreen
Octinoxate 4%Sunscreen

Uses

Warnings

  • 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 or irritation develops and lasts

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

Directions

Other Ingredients

Water, Carthamus Tinctorius (Safflower) Oleosomes, C12-15 Alkyl Benzoate, C13-14 Isoparrafin, Laureth 7, Polyacrylamide, Benzyl Alcohol, Fragrance, Sodium Hydroxide, Methylisothiazolinone, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract, Citric Acid

Skin Cancer/Skin Aging Alert & 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:

This product has been shown to help prevent sun burn, not skin cancer or early skin aging.

Other Information

Store at 15-30°C (59-86°F). Protect the product in this container from excessive heat and or freezing conditions.

Manufactured by:
Pharmco Laboratories Inc. • Titusville, FL 32780
www.pharmcolabs.com • 1.800.635.0712 • Reorder CPL16-3

PRINCIPAL DISPLAY PANEL - 87 g Tube Label

PHARMCO
SKINCARE LABS

Daily Facial
Moisturizer

Broad Spectrum SPF 30+

Net wt. 3 oz. (87 g)

PRINCIPAL DISPLAY PANEL - 87 g Tube Label
DAILY FACIAL MOISTURIZER SPF 35 
octinoxate and avobenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58400-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate40 mg  in 1 g
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone25 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Aloe (UNII: V5VD430YW9)  
Benzyl Alcohol (UNII: LKG8494WBH)  
Carthamus Tinctorius Seed Oleosomes (UNII: 9S60Q72309)  
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)  
C13-14 Isoparaffin (UNII: E4F12ROE70)  
Laureth-7 (UNII: Z95S6G8201)  
Methylisothiazolinone (UNII: 229D0E1QFA)  
Sodium Hydroxide (UNII: 55X04QC32I)  
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58400-007-0187 g in 1 TUBE; Type 0: Not a Combination Product06/01/2012
2NDC:58400-007-023900 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/01/2012
Labeler - Pharmco Laboratories Inc. (096270814)
Establishment
NameAddressID/FEIBusiness Operations
Pharmco Laboratories Inc.096270814MANUFACTURE(58400-007) , LABEL(58400-007) , PACK(58400-007) , ANALYSIS(58400-007)

Revised: 1/2024
Document Id: 15a7def9-02ea-4381-afd4-59901130dd69
Set id: 7bfa0e42-c909-40c3-9f7e-e0c2ca2ba16a
Version: 4
Effective Time: 20240110
 
Pharmco Laboratories Inc.