GOOD SKIN MD FACIAL MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 15- zinc oxide lotion 
The Procter & Gamble Manufacturing Company

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.

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Good Skin MD Facial Moisturizer with Sunscreen Broad Spectrum SPF 15

Drug Facts

ZINC OXIDE 9.7%

Sunscreen

Uses

Warnings

For external use only

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 occurs

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

Directions

Other information

Inactive ingredients

Water, caprylic/capric triglyceride, isohexadecane, glycerin, hydroxyacetophenone, C13-14 isoparaffin, steareth-21, polyhydroxystearic acid, laureth-7, steareth-2, stearyl alcohol, behenyl alcohol, cetyl alcohol, disodium EDTA, polyacrylamide, triethoxycaprylylsilane, phenoxyethanol.

Distr. by: PROCTER & GAMBLE

CINCINNATI, OH 45202

www.getgoodskinmd.com

Questions & comments?

Questions or comments? 888-FAB-3063

PRINCIPAL DISPLAY PANEL - 50 mL Carton

GOOD SKIN MD

DERMATOLOGIST TESTED

Facial Moisturizer

with SUNSCREEN

ZINC OXIDE

BROAD SPECTRUM

SPF 15

50 mL (1.7 FL OZ)

GS

GOOD SKIN MD FACIAL MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 15 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-692
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE9.7 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
LAURETH-7 (UNII: Z95S6G8201)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DOCOSANOL (UNII: 9G1OE216XY)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
STEARETH-21 (UNII: 53J3F32P58)  
STEARETH-2 (UNII: V56DFE46J5)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-692-501 in 1 CARTON03/01/2022
150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02003/01/2022
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 3/2023
Document Id: f6425582-326e-7fb5-e053-2995a90a322a
Set id: f6425582-327f-7fb5-e053-2995a90a322a
Version: 1
Effective Time: 20230306
 
The Procter & Gamble Manufacturing Company