private label super light oil-free spf45

Generic: 2.75% octinsalate, 7.50% octinoxate, 8.00% zinc oxide sunscreen

Labeler: swiss-american cdmo, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name private label super light oil-free spf45
Generic Name 2.75% octinsalate, 7.50% octinoxate, 8.00% zinc oxide sunscreen
Labeler swiss-american cdmo, llc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

octinoxate 75 g/1000g, octisalate 27.5 g/1000g, zinc oxide 80 g/1000g

Manufacturer
Swiss-American CDMO, LLC

Identifiers & Regulatory

Product NDC 60232-0008
Product ID 60232-0008_c9d33e9b-77bd-4ca7-b228-f49318307a70
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2011-03-22

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 602320008
Hyphenated Format 60232-0008

Supplemental Identifiers

UNII
4Y5P7MUD51 4X49Y0596W SOI2LOH54Z

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 private label super light oil-free spf45 (source: ndc)
Generic Name 2.75% octinsalate, 7.50% octinoxate, 8.00% zinc oxide sunscreen (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 75 g/1000g
  • 27.5 g/1000g
  • 80 g/1000g
source: ndc
Packaging
  • 60 g in 1 BOTTLE (60232-0008-2)
source: ndc

Packages (1)

60232-0008-2 60 g in 1 BOTTLE (60232-0008-2)

Ingredients (3)

octinoxate (75 g/1000g) octisalate (27.5 g/1000g) zinc oxide (80 g/1000g)

Linked Drug Pages (1)

Private Label Super Light Oil-Free SPF45 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "c9d33e9b-77bd-4ca7-b228-f49318307a70", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["6a08448a-46bc-4330-ae2d-f716bb4edfa7"], "manufacturer_name": ["Swiss-American CDMO, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 BOTTLE (60232-0008-2)", "package_ndc": "60232-0008-2", "marketing_start_date": "20110322"}], "brand_name": "Private Label Super Light Oil-Free SPF45", "product_id": "60232-0008_c9d33e9b-77bd-4ca7-b228-f49318307a70", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60232-0008", "generic_name": "2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscreen", "labeler_name": "Swiss-American CDMO, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Private Label Super Light Oil-Free SPF45", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 g/1000g"}, {"name": "OCTISALATE", "strength": "27.5 g/1000g"}, {"name": "ZINC OXIDE", "strength": "80 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110322", "listing_expiration_date": "20261231"}