advanced sun resistance spf 30

Generic: homosalate, octinoxate, oxybenzone, octisalate, avobenzone

Labeler: june jacobs labs, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name advanced sun resistance spf 30
Generic Name homosalate, octinoxate, oxybenzone, octisalate, avobenzone
Labeler june jacobs labs, llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

avobenzone 3.371 g/112.38g, homosalate 11.238 g/112.38g, octinoxate 8.429 g/112.38g, octisalate 5.619 g/112.38g, oxybenzone 6.743 g/112.38g

Manufacturer
June Jacobs Labs, LLC

Identifiers & Regulatory

Product NDC 65278-319
Product ID 65278-319_18f879f0-3d5c-0067-e063-6394a90a9db3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2021-03-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65278319
Hyphenated Format 65278-319

Supplemental Identifiers

UNII
G63QQF2NOX V06SV4M95S 4Y5P7MUD51 4X49Y0596W 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 advanced sun resistance spf 30 (source: ndc)
Generic Name homosalate, octinoxate, oxybenzone, octisalate, avobenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 3.371 g/112.38g
  • 11.238 g/112.38g
  • 8.429 g/112.38g
  • 5.619 g/112.38g
  • 6.743 g/112.38g
source: ndc
Packaging
  • 112.38 g in 1 TUBE (65278-319-01)
  • 112.38 g in 1 CARTON (65278-319-02)
source: ndc

Packages (2)

65278-319-01 112.38 g in 1 TUBE (65278-319-01) 65278-319-02 112.38 g in 1 CARTON (65278-319-02)

Ingredients (5)

avobenzone (3.371 g/112.38g) homosalate (11.238 g/112.38g) octinoxate (8.429 g/112.38g) octisalate (5.619 g/112.38g) oxybenzone (6.743 g/112.38g)

Linked Drug Pages (1)

Advanced Sun Resistance SPF 30 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "18f879f0-3d5c-0067-e063-6394a90a9db3", "openfda": {"unii": ["G63QQF2NOX", "V06SV4M95S", "4Y5P7MUD51", "4X49Y0596W", "95OOS7VE0Y"], "spl_set_id": ["18f879f0-3d5b-0067-e063-6394a90a9db3"], "manufacturer_name": ["June Jacobs Labs, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "112.38 g in 1 TUBE (65278-319-01)", "package_ndc": "65278-319-01", "marketing_start_date": "20210320"}, {"sample": false, "description": "112.38 g in 1 CARTON (65278-319-02)", "package_ndc": "65278-319-02", "marketing_start_date": "20210320"}], "brand_name": "Advanced Sun Resistance SPF 30", "product_id": "65278-319_18f879f0-3d5c-0067-e063-6394a90a9db3", "dosage_form": "CREAM", "product_ndc": "65278-319", "generic_name": "Homosalate, Octinoxate, Oxybenzone, Octisalate, Avobenzone", "labeler_name": "June Jacobs Labs, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advanced Sun Resistance SPF 30", "active_ingredients": [{"name": "AVOBENZONE", "strength": "3.371 g/112.38g"}, {"name": "HOMOSALATE", "strength": "11.238 g/112.38g"}, {"name": "OCTINOXATE", "strength": "8.429 g/112.38g"}, {"name": "OCTISALATE", "strength": "5.619 g/112.38g"}, {"name": "OXYBENZONE", "strength": "6.743 g/112.38g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210320", "listing_expiration_date": "20261231"}