skinpharmacy advanced sun therapy broad spectrum spf 50 face

Generic: homosalate, oxybenzone, octisalate, avobenzone, octocrylene

Labeler: cvs health
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name skinpharmacy advanced sun therapy broad spectrum spf 50 face
Generic Name homosalate, oxybenzone, octisalate, avobenzone, octocrylene
Labeler cvs health
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

avobenzone 30 mg/mL, homosalate 100 mg/mL, octisalate 50 mg/mL, octocrylene 20 mg/mL, oxybenzone 60 mg/mL

Manufacturer
CVS Health

Identifiers & Regulatory

Product NDC 69842-021
Product ID 69842-021_869054ce-7c49-458f-95b0-7a042ed0adbb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part352
Listing Expiration 2026-12-31
Marketing Start 2016-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842021
Hyphenated Format 69842-021

Supplemental Identifiers

UNII
G63QQF2NOX V06SV4M95S 4X49Y0596W 5A68WGF6WM 95OOS7VE0Y

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 skinpharmacy advanced sun therapy broad spectrum spf 50 face (source: ndc)
Generic Name homosalate, oxybenzone, octisalate, avobenzone, octocrylene (source: ndc)
Application Number part352 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
  • 100 mg/mL
  • 50 mg/mL
  • 20 mg/mL
  • 60 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (69842-021-01) / 90 mL in 1 TUBE
source: ndc

Packages (1)

69842-021-01 1 TUBE in 1 CARTON (69842-021-01) / 90 mL in 1 TUBE

Ingredients (5)

avobenzone (30 mg/mL) homosalate (100 mg/mL) octisalate (50 mg/mL) octocrylene (20 mg/mL) oxybenzone (60 mg/mL)

Linked Drug Pages (1)

SkinPharmacy Advanced Sun Therapy Broad Spectrum SPF 50 Face ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "869054ce-7c49-458f-95b0-7a042ed0adbb", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "95OOS7VE0Y"], "spl_set_id": ["efbdfe0e-c602-48f6-9faf-dc85298f1741"], "manufacturer_name": ["CVS Health"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69842-021-01)  / 90 mL in 1 TUBE", "package_ndc": "69842-021-01", "marketing_start_date": "20160401"}], "brand_name": "SkinPharmacy Advanced Sun Therapy Broad Spectrum SPF 50 Face", "product_id": "69842-021_869054ce-7c49-458f-95b0-7a042ed0adbb", "dosage_form": "LIQUID", "product_ndc": "69842-021", "generic_name": "homosalate, oxybenzone, octisalate, avobenzone, octocrylene", "labeler_name": "CVS Health", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SkinPharmacy Advanced Sun Therapy Broad Spectrum SPF 50 Face", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "20 mg/mL"}, {"name": "OXYBENZONE", "strength": "60 mg/mL"}], "application_number": "part352", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}