ALL DAY MOISTURIZING SPF 15 EQB- octinoxate 6% zinc oxide 3% lotion 
Walmart

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PLSF-1844 EQB All Day Moisturizing Lotion SPF 15 (DMI)

Active ingredients                         Purpose

Octinoxate, 6%                               Sunscreen
Zinc Oxide, 3%                              Sunscreen

Uses

•helps prevent sunburn• If used as directed with other sun protection measures (see Oirections),decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings
For external use only

Do not use on

• damaged or broken skin.

When using this product 

•keep out of eyes. Rinse with waterto remove.

Stop use and ask a doctor

• if rash occurs.

Keep out of reach of children. If swallowed,get medical help orcontact a Poison Control Center right away

Directions:

• apply liberal 15 minutes before sun exposure• reapply at least every 2 hours •use a water resistant sunscreen if swimmingor sweating•children under 6 months of age: ask a doctor• Sun Protection Measures:Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk. regularly usea sunscreen wrtha Broad Spectrum SPF value of15 or higher and other suncrin protection measures including:
• limrt time in the sun, especial from 10a.m. -2 p.rn.•wear long-sleeve shorts , pants, hats and sunglasses

Inactive Ingredients:

Water
Xanthan Gum
Disodium EDTA
Glycerin
Isohexadecane
Cyclopentasiloxane
Steareth-21
Stearyl Alcohol
Cetyl Alcohol
Steareth-2
Potassium Cetyl Phosphate
Octinoxate
Zinc Oxide, Triethoxycaprylylsilane
Tocopheryl Acetate
Behenyl Alcohol
Phenoxyethanol, Ethylhexylglycerin
Panthenol
Polyacrylamide, C13-14 Isoparaffin, Laureth-7
Sodium Polyacrylate, Dimethicone, Cyclopentasiloxane, Trideceth-6, PEG/PPG-18/18 Dimethicone
Aminomethyl Propanol
Aloe Barbadensis (Aloe Vera) Leaf Juice, Sodium Benzoate, Potassium Sorbate

image description

ALL DAY MOISTURIZING SPF 15  EQB
octinoxate 6% zinc oxide 3% lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-210
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE6 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
STEARETH-2 (UNII: V56DFE46J5)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
STEARETH-21 (UNII: 53J3F32P58)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
DOCOSANOL (UNII: 9G1OE216XY)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
LAURETH-7 (UNII: Z95S6G8201)  
ALOE (UNII: V5VD430YW9)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PANTHENOL (UNII: WV9CM0O67Z)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-210-061 in 1 CARTON10/17/2023
1177 mL in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/09/2023
Labeler - Walmart (051957769)
Registrant - Bridgeview Investments, LLC (035014854)
Establishment
NameAddressID/FEIBusiness Operations
Dimensional Merchandising Inc076693183manufacture(79903-210)

Revised: 10/2023
Document Id: 07ef707a-f9e7-42b0-e063-6294a90acce9
Set id: c09a59ca-97d0-4a74-9c10-31a939472fc6
Version: 2
Effective Time: 20231017
 
Walmart