FDA.reportPublic FDA data

L'Bri Pure N' Natural Diaper Cream

Manufacturer
L'Bri Health and Beauty
Effective date
2017-10-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:28

Label at a glance#

ProductLBri Pure N Natural Diaper
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

Helps treat and prevent diaper rash. Protects chafed skin associated with diaper rash and helps protect from wetness.

Dosage and administration

Change wet and soiled diapers promptly Cleanse the diaper area and allow to dry. Apply cream liberally and as often as necessary, with each diaper change, especially at bedtime or when exposure to wet diapers may be prolonged.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 20%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

  • Helps treat and prevent diaper rash.
  • Protects chafed skin associated with diaper rash and helps protect from wetness.

Warnings

WARNINGS SECTION

  • For external use only

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • Condition worsens.
  • Symptoms last more than 7 days, or clear up and occur again within a few days.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Change wet and soiled diapers promptly
  • Cleanse the diaper area and allow to dry.
  • Apply cream liberally and as often as necessary, with each diaper change, especially at bedtime or when exposure to wet diapers may be prolonged.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Butyrospermum Parkii (Shea) Butter, Carbomer, Cetyl Alcohol, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Octyl Palmitate, Parfum (Natural Fragrace), Phenoxyethanol, Polysorbate-20, Sodium Hydroxide, Stearic Acid, Stearyl Alcohl, Tocopheryl Acetate (Vitamin E).

Other information

SPL UNCLASSIFIED SECTION

Store between 20° to 30°C (68° to 86°F)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 1282401Label6.jpg

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71238-85771238-857-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
SHEA BUTTERK49155WL9YIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
ETHYLHEXYL PALMITATE2865993309IACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
SODIUM HYDROXIDE55X04QC32IIACT
STEARIC ACID4ELV7Z65APIACT
STEARYL ALCOHOL2KR89I4H1YIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ZINC OXIDESOI2LOH54ZACTIM

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
0724e37d-cc7a-66a4-e063-6394a90a8661999fe072-48cf-43e2-9a1a-3b13dc0c3e832023-10-07WarningsExact identifier
spl set id: 999fe072-48cf-43e2-9a1a-3b13dc0c3e83

Reported adverse events (FAERS/openFDA)#

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