Jardient TALLOW SUNSCREEN

Manufacturer
GLOWVERA
Effective date
2025-11-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:42:36

Label at a glance#

ProductJardient TALLOW SUNSCREEN
Active ingredientZINC OXIDE
Label structure13 sections

Dosage and administration

.apply liberally 15 minutes before sun exposure. .reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours children after 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 of 15 or higher and other sun protec...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Non-Nano Zinc Oxide 25%

use

INDICATIONS & USAGE SECTION

.helps prevent sunburn

.if used as directed with other sun protectionmeasures(see Directions),decreases therisk of skin cancer and early skin agingcaused by the sun

Warning

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 doctorif rash occurs.

.Keep out of reach of children.lf product isswallowed, get medical help or contact aPoison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

.apply liberally 15 minutes before sun exposure.

.reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours

children after 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 of 15 or higher and other sun protection.

measures including:

-limit time in the sun, especially from10am-2pm

-wear long-sleeve shirts, pants, hats, and sunglasses

Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Tallow, Tocopherol(vitamin E),Centella Asiatica extract, Camellia Sinensisleaf extract, Rosmarinus Officinalis leafextract,Jojoba Esters, Lecithin, CeraAlba(beeswax),Glycerin,Titanium Dioxide.Cetyl Alcohol, Dioctyl Carbonate, Silica,Polyglycerol-10 Decaoleate.

none

OTC - ASK DOCTOR SECTION

none

none

OTC - DO NOT USE SECTION

none

none

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

none

none

OTC - STOP USE SECTION

none

none

OTC - WHEN USING SECTION

none

Questions?

OTC - QUESTIONS SECTION

support@jardients.com

Purpose

OTC - PURPOSE SECTION

Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128X004M8IJBTlabel.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85646-005-01Jardient TALLOW SUNSCREEN85 g in 1 BOTTLECREAM851
85646-005-01Jardient TALLOW SUNSCREEN1 in 1 BOXCREAM11

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85646-00585646-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
43013b33-8863-5253-e063-6294a90a90ed43013b21-b3de-6d98-e063-6394a90adb802025-11-07WarningsExact identifier
spl id: 43013b33-8863-5253-e063-6294a90a90ed
spl set id: 43013b21-b3de-6d98-e063-6394a90adb80

Reported adverse events (FAERS/openFDA)#

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