private label spf45 water resistant paraben free sunscreen

Generic: octinoxate, octisalate, 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 spf45 water resistant paraben free sunscreen
Generic Name octinoxate, octisalate, zinc oxide sunscreen
Labeler swiss-american cdmo, llc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

octinoxate 75 g/1000g, octisalate 30 g/1000g, zinc oxide 80 g/1000g

Manufacturer
Swiss-American CDMO, LLC

Identifiers & Regulatory

Product NDC 60232-0006
Product ID 60232-0006_21e18883-f579-425a-a460-1e601e1b30be
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2011-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 602320006
Hyphenated Format 60232-0006

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 spf45 water resistant paraben free sunscreen (source: ndc)
Generic Name octinoxate, octisalate, zinc oxide sunscreen (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 75 g/1000g
  • 30 g/1000g
  • 80 g/1000g
source: ndc
Packaging
  • 50 g in 1 BOTTLE (60232-0006-1)
source: ndc

Packages (1)

60232-0006-1 50 g in 1 BOTTLE (60232-0006-1)

Ingredients (3)

octinoxate (75 g/1000g) octisalate (30 g/1000g) zinc oxide (80 g/1000g)

Linked Drug Pages (1)

Private Label SPF45 Water Resistant Paraben Free Sunscreen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "21e18883-f579-425a-a460-1e601e1b30be", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["f997f4fc-7da5-433c-9a53-2030b489b4f6"], "manufacturer_name": ["Swiss-American CDMO, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (60232-0006-1)", "package_ndc": "60232-0006-1", "marketing_start_date": "20110831"}], "brand_name": "Private Label SPF45 Water Resistant Paraben Free Sunscreen", "product_id": "60232-0006_21e18883-f579-425a-a460-1e601e1b30be", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "60232-0006", "generic_name": "Octinoxate, Octisalate, Zinc Oxide Sunscreen", "labeler_name": "Swiss-American CDMO, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Private Label SPF45 Water Resistant Paraben Free Sunscreen", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 g/1000g"}, {"name": "OCTISALATE", "strength": "30 g/1000g"}, {"name": "ZINC OXIDE", "strength": "80 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110831", "listing_expiration_date": "20261231"}