Shopping Annuity Brand Premium Sunscreen

Shopping Annuity Brand Premium Sunscreen by

Drug Labeling and Warnings

Shopping Annuity Brand Premium Sunscreen by is a Otc medication manufactured, distributed, or labeled by Market America, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SHOPPING ANNUITY BRAND PREMIUM SUNSCREEN- zinc oxide cream 
Market America, Inc.

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Shopping Annuity Brand Premium Sunscreen

Drug Facts

Active ingredient

Zinc Oxide (20%)

Purpose

Sunscreen

Uses

• Helps prevent sunburn

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 swallowed, get medical help or contact a poison control center immediately.

Directions

• Apply generously 15 minutes before sun exposure 
• Reapply at least every 2 hours
• Use a water-resistant sunscreen if swimming or sweating
• Children under 6 months of age: ask a doctor

• limit time in the sun, especially from 10 a.m.-2 p.m.
• wear long-sleeved shirts, pants, hats and sunglasses

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: Sun Protection Measures:

Inactive ingredients

Water (Aqua), Coco-Caprylate/Caprate, Glycerin, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Cetearyl Glucoside, Glyceryl Caprylate, Glyceryl Undecylenate, Polyhydroxystearic Acid, Microcrystalline Cellulose, Xanthan Gum, Tocopheryl Acetate, Citrullus Lanatus (Watermelon) Fruit Extract, Sodium Hydroxide, Lens Esculenta (Lentil) Fruit Extract, Phytic Acid, Allantoin, Pyrus Malus (Apple) Fruit Extract, Sodium Lactate, Sodium PCA, Sodium Benzoate, Potassium Sorbate, Citric Acid

Other information

• Protect this product from excessive heat and direct sun

Package Labeling:

SHOPPING ANNUITY BRAND PREMIUM SUNSCREEN 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76209-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	200 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
GLYCERIN (UNII: PDC6A3C0OX)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
XANTHAN GUM (UNII: TTV12P4NEE)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATERMELON (UNII: 231473QB6R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LENS CULINARIS FRUIT (UNII: ZYZ076G9JH)
FYTIC ACID (UNII: 7IGF0S7R8I)
ALLANTOIN (UNII: 344S277G0Z)
APPLE (UNII: B423VGH5S9)
SODIUM LACTATE (UNII: TU7HW0W0QT)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76209-001-01	118 mL in 1 TUBE; Type 0: Not a Combination Product	02/17/2021	03/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/17/2021	03/31/2022

Labeler - Market America, Inc. (797412236)

Revised: 2/2024

Document Id: 1133195c-f2d0-a846-e063-6294a90ac44f

34390-5

Set id: b957cdc9-2730-cf47-e053-2a95a90a9998

Version: 3

Effective Time: 20240212