FDA.reportPublic FDA data

Natural Diaper Rash

Manufacturer
Products On The Go, LLC
Effective date
2017-05-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:16:21

Label at a glance#

ProductNatural Diaper Rash
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

Helps treat and prevent diaper rash. Protects chafed skin and minor irritation associated with diaper rash. Helps seal out wetness.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 12%

OTC - PURPOSE SECTION

Skin Protection

Uses:

INDICATIONS & USAGE SECTION

  • Helps treat and prevent diaper rash.
  • Protects chafed skin and minor irritation associated with diaper rash.
  • Helps seal out wetness.

WARNINGS:

WARNINGS SECTION

For external use only.

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • Conditions worsen.
  • Symptoms last more then seven days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help immediately or contact poison control center right away.

DIRECTION:

DOSAGE & ADMINISTRATION SECTION

  • Change wet and soiled diapers promptly.
  • Cleans the diaper area and allow to dry.
  • Apply cream liberally, as often as necessary, with each diaper change, especially at bed time or before any prolonged exposure to wet diapers.

Other infomation:

SPL UNCLASSIFIED SECTION

Store at 15° -30° C [59°-86°)

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera) Extract, Beeswax, Butyrospermum Parkii (Shea) Butter, Calendula Officinalis Extract, Chamomilla Recutita (Chamomile) Oil, Cocos Nucifera (Coconut) Oil, Cucumis Sativus (Cucumber) Extract, Glycyrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Oil, Lavandula Angustifolia (Lavendar) Oil, Tocopheryl Acetate (Vitamin E).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70668-82770668-827-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
YELLOW WAX2ZA36H0S2VIACT
SHEA BUTTERK49155WL9YIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
CHAMOMILEFGL3685T2XIACT
COCONUT OILQ9L0O73W7LIACT
CUCUMBERYY7C30VXJTIACT
GLYCYRRHIZA GLABRA2788Z9758HIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
LAVENDER OILZBP1YXW0H8IACT
.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
074334af-c26d-4126-e063-6394a90ae4c44fa7948f-5089-3aa6-e054-00144ff8d46c2023-10-09WarningsExact identifier
spl set id: 4fa7948f-5089-3aa6-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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