FDA.reportPublic FDA data

CONDITION AND ENHANCE PHYSICAL UV BLOCK

Manufacturer
OMP, Inc. | Swiss-American Products
Effective date
2011-12-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:49:54

Label at a glance#

ProductCONDITION AND ENHANCE PHYSICAL UV BLOCK SPF 32
Active ingredientZINC OXIDE
Label structure8 sections

Dosage and administration

Apply liberally to all exposed areas 15 minutes prior to sun exposure and as needed. For children less than six months of age, consult a physician.

Storage and handling

Store at controlled room temperature: 15°-30°C (59°-86°F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 18.5%.

Warning

WARNINGS SECTION

For external use only.

See bottom of outer package.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally to all exposed areas 15 minutes prior to sun exposure and as needed.
  • For children less than six months of age, consult a physician.

Other Information

STORAGE AND HANDLING SECTION

Store at controlled room temperature: 15°-30°C (59°-86°F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

See bottom of outer package.

SPL UNCLASSIFIED SECTION

Dist. by OMP Inc. Long Beach, CA 90802

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OBAGI®
MEDICAL

CONDITION & ENHANCE

AM 6

physical uv block

SPF 32

Broad-Spectrum UVA/UVB
Physical Sunblock
18.5% Zinc Oxide

NET WT. 2 OZ. (57 g)

Principal Display Panel - 57 g Bottle Label
Principal Display Panel - 57 g Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62032-118-362019-11-13C16284748780-197449f38-d589-f6ea-e053-dbdaa90aa703OBAGI ® MEDICAL CONDITION & ENHANCE physical uv block SPF 32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62032-118CONDITION AND ENHANCE PHYSICAL UV BLOCK SPF 32 (ZINC OXIDE) CREAM [OMP, INC.]1Legacy NDC20111230_4cd816f1-af26-491e-917f-93399b2e33c1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62032-11862032-118-36

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
ZINC OXIDESOI2LOH54ZACTIB
ISOPROPYL PALMITATE8CRQ2TH63MIACT
WATER059QF0KO0RIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
YELLOW WAX2ZA36H0S2VIACT
GLYCERETH-26NNE56F2N14IACT
SODIUM CHLORIDE451W47IQ8XIACT
METHYLPARABENA2I8C7HI9TIACT
DIMETHICONE92RU3N3Y1OIACT
PROPYLPARABENZ8IX2SC1OHIACT
EDETATE DISODIUM7FLD91C86KIACT
EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP08H094218DIACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5)035JKJ76MTIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT

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
8480c4f0-5b62-4d18-840d-99831c9a6dfe4cd816f1-af26-491e-917f-93399b2e33c12026-02-12WarningsExact identifier
spl set id: 4cd816f1-af26-491e-917f-93399b2e33c1

Reported adverse events (FAERS/openFDA)#

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