Double-Duty Face Moisturizer

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Double-Duty Face Moisturizer
Generic name: MOSITURIZING SUNSCREEN
Manufacturer: Jack Black, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 672be406-e3a1-47b4-8ef6-ee2b62baae96
SPL ID: 5aff192a-cd63-e163-e063-6294a90ab621
Version: 9
Effective date: 2026-09-08
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:50

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Double-Duty Face Moisturizer	openfda.brand_name
generic name		MOSITURIZING SUNSCREEN	openfda.generic_name
manufacturer name		Jack Black, LLC	openfda.manufacturer_name
ndc	package	66738-020-02	openfda.package_ndc
ndc	package	66738-020-19	openfda.package_ndc
ndc	package	66738-020-03	openfda.package_ndc
ndc	package	66738-020-04	openfda.package_ndc
ndc	package	66738-020-50	openfda.package_ndc
ndc	package	66738-020-01	openfda.package_ndc
ndc	package	66738-020-16	openfda.package_ndc
ndc	product	66738-020	openfda.product_ndc
ndc11	package	66738002001	derived:openfda.package_ndc
ndc11	package	66738002003	derived:openfda.package_ndc
ndc11	package	66738002050	derived:openfda.package_ndc
ndc11	package	66738002019	derived:openfda.package_ndc
ndc11	package	66738002004	derived:openfda.package_ndc
ndc11	package	66738002002	derived:openfda.package_ndc
ndc11	package	66738002016	derived:openfda.package_ndc
spl id		5aff192a-cd63-e163-e063-6294a90ab621	id
spl set id		672be406-e3a1-47b4-8ef6-ee2b62baae96	set_id
unii		G63QQF2NOX	openfda.unii
unii		4Y5P7MUD51	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use on damaged or broken skin Stop use and ask doctor if rash occurs When using this product keep out of eyes. Rinse with water to remove Keep out of reach of children If swallowed, get medical help or contact Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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