Bali Body Coconut Lip Balm SPF 15

Manufacturer
Bali Body Pty Ltd
Effective date
2019-08-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:14:34

Label at a glance#

ProductBali Body Coconut Lip Balm SPF 15
Active ingredientOCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bali Body Lip BalmBali Body Lip BalmBali Body Lip Balm OuterBali Body Lip Balm Outer

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2%

Homosalate 2.8%

Avobenzone 2%

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PURPOSE SECTION

A multi-tasking beauty cream.

Provides SPF 15 protection.

INDICATIONS & USAGE SECTION

Shake well before use. Apply liberaly 15 minutes before sun exposure.

Children under 6 months old: Ask a doctor.

Re-apply every 2 hours.

Use water-resistant sunscreen if swimming or sweating.

Store in cool dry place.

INACTIVE INGREDIENT SECTION

WARNINGS SECTION

Skin Cancer/Skin Ageing Alert: Spending time in the sun increases your risk of skin cancer and early skin aging.

This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

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.

Always wear a hat, protective clothing and sunglasses.

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70630-1701-12021-05-14C16284748780-1ba0f9c33-5ab4-a910-e053-dadaa90a0b85Bali Body Coconut Lip Balm SPF 15
70630-1701-12021-01-29C16284748780-1ba0f9c33-5ab4-a910-e053-dadaa90a0b85Bali Body Coconut Lip Balm SPF 15

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70630-170170630-1701-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
b8392126-4c53-de19-e053-2995a90a73e050aa6562-905a-4802-e054-00144ff88e882021-01-06WarningsExact identifier
spl set id: 50aa6562-905a-4802-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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