Shopping Annuity Brand Premium Sunscreen

Manufacturer
Market America, Inc.
Effective date
2023-10-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:23:24

Label at a glance#

ProductShopping Annuity Brand Premium Sunscreen
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

Helps prevent sunburn

Dosage and administration

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 sunscree...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide (20%)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

  • Protect this product from excessive heat and direct sun

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76209-00176209-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1133195c-f2d0-a846-e063-6294a90ac44fb957cdc9-2730-cf47-e053-2a95a90a99982024-02-12WarningsExact identifier
spl set id: b957cdc9-2730-cf47-e053-2a95a90a9998

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.