Guards Up

Manufacturer
Offspring Beauty Co
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:34

Label at a glance#

ProductGuards Up Daily
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

apply liberally and evenly 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating, immediately after toweling drying and at least every 2 hours children under 6 months of age: ask a doctor 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 Br...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 15.2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

  • 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally and evenly 15 minutes before sun exposure
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating, immediately after toweling drying and at least every 2 hours
  • children under 6 months of age: ask a doctor
  • 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 othe sun protection measures including: limit time in sun, especially from 10 a.m. to 2 p.m. and wear long-sleeved shirts, pants, hats, and sunglasses

Other information

OTHER SAFETY INFORMATION

protect this product in this container from excessive heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Butyloctyl Salicylate, Isodecyl Neopentanoate, Calcium Sodium Borosilicate, Diheptyl Succinate, C18-21 Alkane, Erythritol, Cetearly Alcohol, Sodium Stearoyl Glutamate, Capryloyl Glycerin/Sebacic Acid Copolymer, Propanediol, Archidyl Alcohol, Glycerin, Pyrus Malus (Apple) Fruit Extract, Caprylic/Capric Triglyceride, Tocopherol, Caprylyl Glycol, Coco-Glucoside, Ethyl Ferulate, Behenyl Alcohol, Cetyl Alcohol, Archidyl Glucoside, Bisabolol, Polyhydroxystearic Acid, Citric Acid, Sodium Gluconate, Xanthan Gum, Octyldodecyl Oleate, Caprylhydroxamic Acid, Hydrolyzed Jojoba Esters, Sodium Hyaluronate, Crithmum Maritimum Extract, Maltodextrin, Moringa Oleifera Seed Extract, Aloe Barbadensis Leaf, Iron Oxides (CI 77491, CI 77492).

1.7 fl oz tube label and Unit Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unit CartonUnit CartonTubeTube

Products#

Every source-derived product name is available through these pages.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73690-02573690-025-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 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
f200f199-23f1-e140-e053-2995a90aeffda35a232f-7e7b-5237-e053-2a95a90a89862023-01-11WarningsExact identifier
spl set id: a35a232f-7e7b-5237-e053-2a95a90a8986

Reported adverse events (FAERS/openFDA)#

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