hampton sun

Generic: octinoxate, oxybenzone

Labeler: hampton sun
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name hampton sun
Generic Name octinoxate, oxybenzone
Labeler hampton sun
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

octinoxate 4 g/100g, oxybenzone 2 g/100g

Manufacturer
Hampton Sun

Identifiers & Regulatory

Product NDC 87170-001
Product ID 87170-001_41ed609c-2ab8-057e-e063-6294a90a7ee9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2025-08-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 87170001
Hyphenated Format 87170-001

Supplemental Identifiers

UPC
0184573000015
UNII
4Y5P7MUD51 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 hampton sun (source: ndc)
Generic Name octinoxate, oxybenzone (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 4 g/100g
  • 2 g/100g
source: ndc
Packaging
  • 118 g in 1 BOTTLE, PLASTIC (87170-001-01)
source: ndc

Packages (1)

87170-001-01 118 g in 1 BOTTLE, PLASTIC (87170-001-01)

Ingredients (2)

octinoxate (4 g/100g) oxybenzone (2 g/100g)

Linked Drug Pages (1)

HAMPTON SUN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "41ed609c-2ab8-057e-e063-6294a90a7ee9", "openfda": {"upc": ["0184573000015"], "unii": ["4Y5P7MUD51", "95OOS7VE0Y"], "spl_set_id": ["a5e7efb4-cf14-4ffa-ae7b-470653d8e6f6"], "manufacturer_name": ["Hampton Sun"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 g in 1 BOTTLE, PLASTIC (87170-001-01)", "package_ndc": "87170-001-01", "marketing_start_date": "20250822"}], "brand_name": "HAMPTON SUN", "product_id": "87170-001_41ed609c-2ab8-057e-e063-6294a90a7ee9", "dosage_form": "GEL", "product_ndc": "87170-001", "generic_name": "Octinoxate, Oxybenzone", "labeler_name": "Hampton Sun", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HAMPTON SUN", "active_ingredients": [{"name": "OCTINOXATE", "strength": "4 g/100g"}, {"name": "OXYBENZONE", "strength": "2 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250822", "listing_expiration_date": "20261231"}