Revlon Kiss Balm SPF 20

Manufacturer
Revlon Consumer Products Corp | REVLON, INC.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:49:53

Label at a glance#

ProductRevlon Kiss Balm SPF 20
Active ingredientAVOBENZONE, OCTINOXATE, OXYBENZONE
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.0%

Octinoxate 7.5%

Oxybenzone 3.0%

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Polybutene, Diisostearyl Malate, Isononyl Isononanoate, Bis-Diglyceryl Polyacyladipate-2, Octyldodecyl Neopentanoate, Polyethylene, Ozokerite, Diisopropyl Dimer Dilinoleate, Cera Alba ((Beeswax) Cire D Abeille), Parfum (Fragrance), Flavor, Punica Granatum Seed Oil, Rubus Idaeus (Raspberry) Seed Oil, Vitis Vinifera (Grape) Seed Oil, Calcium Aluminum Borosilicate, Euphorbia Cerifera (Candelilla) Wax, Cetyl Palmitate, Benzoic Acid, Oxidized Polyethylene, BHT, Silica, Sodium Saccharin, Benzyl Benzoate, Limonene, Benzyl Alcohol, Citral, Amyl Cinnamal, Hexyl Cinnamal, Hydroxycitronellal, Alpha-Isomethyl Ionone, Linalool

May Contain- Mica, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, 77492, 77499), Red 6 Lake (CI 15850), Red 7 Lake (CI 15850), Red 28 Lake (CI 45410), Red 33 Lake (CI 17200), Blue 1 Lake (CI 42090), Yellow 5 Lake (CI 19140), Yellow 6 Lake (CI 15985), Carmine (CI 75470

EXTERNAL USE ONLY

WARNINGS SECTION

External Use Only

Questions?

OTC - QUESTIONS SECTION

1-800-473-8566

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure.

INDICATIONS & USAGE SECTION

Helps prevent sunbunrs. If used as directed with other sun protection measures (See Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

OTC - PURPOSE SECTION

Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Revlon Kiss BalmRevlon Kiss BalmRevlon Kiss Balm SPF 20

Broad Spectrum

Avobenzone- 2.0%

Octinoxate - 7.5%

Oxybenzone- 3.0%

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10967-640-19Revlon Kiss Balm SPF 202.6 mL in 1 CONTAINERSTICK2.63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10967-640REVLON KISS BALM SPF 20 (AVOBENZONE, BENZOPHENONE-3, OCTINOXATE) STICK [REVLON CONSUMER PRODUCTS CORP]3Current NDC, Legacy NDC, 1 package rows20250101_410d1cb2-6c90-1ca3-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10967-64010967-640-19

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
Revlon Kiss Balm SPF 20AVOBENZONE, BENZOPHENONE-3, OCTINOXATERevlon Consumer Products Corp410d1cb2-6c90-1ca3-e054-00144ff8d46c2024-12-31WarningsExact identifier
ndc (package): 10967-640-19
ndc (product): 10967-640
ndc11 (package): 10967064019
spl id: 2a96b135-ba7b-6bfd-e063-6294a90a6fa1
spl set id: 410d1cb2-6c90-1ca3-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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