FDA.reportPublic FDA data

Baby Love Personal Care

Manufacturer
Delta Brands Inc
Effective date
2023-09-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:26:20

Label at a glance#

ProductBaby Love Personal Care Diaper Rash
Active ingredientZINC OXIDE
Label structure11 sections

Indications and uses

■ helps treat and prevent diaper rash ■ protects chafed skin due to diaper rash and helps seal out wetness

Dosage and administration

■ change wet and soiled diapers promptly ■ cleanse the diaper area ■ allow to dry ■ apply paste liberally as often as necessary; with each diaper change, specially at bedtime or anytime when exposure to wet diapers may be prolonged

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc oxide 40%

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

■ helps treat and prevent diaper rash

■ protects chafed skin due to diaper rash and helps seal out wetness

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

■ do not get into eyes

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

■ allow to dry

■ apply paste liberally as often as necessary; with each diaper change, specially at bedtime or anytime when exposure to wet diapers may be prolonged

Other Information

SPL UNCLASSIFIED SECTION

■ store at 20º to 25°C (68° to 77°F)

■ do not use if tube seal under cap is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

petrolatum, cod liver oil, lanolin, talc, glycerin, sorbitan sesquioleate, beeswax, tocopheryl acetate, fragrance

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-32020276-320-20, 20276-320-02, 20276-320-45, 20276-320-04, 20276-320-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
COD LIVER OILBBL281NWFGIACT
PETROLATUM4T6H12BN9UIACT
LANOLIN7EV65EAW6HIACT
TALC7SEV7J4R1UIACT
GLYCERINPDC6A3C0OXIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
SYNTHETIC BEESWAX08MNR5YE2RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
04cad5ea-ec4f-d17a-e063-6294a90a68f5c702eedb-c2de-b1db-e053-2a95a90a51292023-09-07WarningsExact identifier
spl id: 04cad5ea-ec4f-d17a-e063-6294a90a68f5
spl set id: c702eedb-c2de-b1db-e053-2a95a90a5129

Reported adverse events (FAERS/openFDA)#

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