up and up illuminating daily moisturizer with sunscreen broad spectrum spf 15

Generic: avobenzone, octinoxate, octisalate

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name up and up illuminating daily moisturizer with sunscreen broad spectrum spf 15
Generic Name avobenzone, octinoxate, octisalate
Labeler target corporation
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, octinoxate 75 mg/mL, octisalate 20 mg/mL

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-934
Product ID 11673-934_2476623c-2e31-7a6b-e063-6294a90aea58
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2013-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673934
Hyphenated Format 11673-934

Supplemental Identifiers

UNII
G63QQF2NOX 4Y5P7MUD51 4X49Y0596W

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name up and up illuminating daily moisturizer with sunscreen broad spectrum spf 15 (source: ndc)
Generic Name avobenzone, octinoxate, octisalate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
  • 75 mg/mL
  • 20 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-934-05) / 118.3 mL in 1 BOTTLE (11673-934-04)
source: ndc

Packages (1)

Ingredients (3)

avobenzone (30 mg/mL) octinoxate (75 mg/mL) octisalate (20 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2476623c-2e31-7a6b-e063-6294a90aea58", "openfda": {"unii": ["G63QQF2NOX", "4Y5P7MUD51", "4X49Y0596W"], "spl_set_id": ["9407a4a9-8a72-6a01-e053-2a95a90a231d"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-934-05)  / 118.3 mL in 1 BOTTLE (11673-934-04)", "package_ndc": "11673-934-05", "marketing_start_date": "20130201"}], "brand_name": "Up and Up Illuminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15", "product_id": "11673-934_2476623c-2e31-7a6b-e063-6294a90aea58", "dosage_form": "LOTION", "product_ndc": "11673-934", "generic_name": "Avobenzone, Octinoxate, Octisalate", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up", "brand_name_suffix": "Illuminating Daily Moisturizer with Sunscreen Broad Spectrum SPF 15", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "OCTINOXATE", "strength": "75 mg/mL"}, {"name": "OCTISALATE", "strength": "20 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130201", "listing_expiration_date": "20261231"}