sundrops 75

Generic: alcohol

Labeler: sunburst chemicals, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sundrops 75
Generic Name alcohol
Labeler sunburst chemicals, inc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

alcohol .6 mL/mL

Manufacturer
Sunburst Chemicals, Inc.

Identifiers & Regulatory

Product NDC 63621-356
Product ID 63621-356_435330fc-c021-151b-e063-6394a90a229b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2009-10-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63621356
Hyphenated Format 63621-356

Supplemental Identifiers

RxCUI
581658
UNII
3K9958V90M

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 sundrops 75 (source: ndc)
Generic Name alcohol (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .6 mL/mL
source: ndc
Packaging
  • 3785 mL in 1 BOTTLE, PLASTIC (63621-356-14)
  • 8 BAG in 1 BOX (63621-356-20) / 1000 mL in 1 BAG
  • 12 BOTTLE, PUMP in 1 BOX (63621-356-25) / 236.6 mL in 1 BOTTLE, PUMP
  • 4 BAG in 1 BOX (63621-356-40) / 1000 mL in 1 BAG
  • 473.2 mL in 1 BOTTLE, PUMP (63621-356-50)
source: ndc

Packages (5)

63621-356-14 3785 mL in 1 BOTTLE, PLASTIC (63621-356-14) 63621-356-20 8 BAG in 1 BOX (63621-356-20) / 1000 mL in 1 BAG 63621-356-25 12 BOTTLE, PUMP in 1 BOX (63621-356-25) / 236.6 mL in 1 BOTTLE, PUMP 63621-356-40 4 BAG in 1 BOX (63621-356-40) / 1000 mL in 1 BAG 63621-356-50 473.2 mL in 1 BOTTLE, PUMP (63621-356-50)

Ingredients (1)

alcohol (.6 mL/mL)

Linked Drug Pages (1)

SunDrops 75 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "435330fc-c021-151b-e063-6394a90a229b", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581658"], "spl_set_id": ["b0623424-939e-4b49-aa99-c1ef22cf0f2d"], "manufacturer_name": ["Sunburst Chemicals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3785 mL in 1 BOTTLE, PLASTIC (63621-356-14)", "package_ndc": "63621-356-14", "marketing_start_date": "20200507"}, {"sample": false, "description": "8 BAG in 1 BOX (63621-356-20)  / 1000 mL in 1 BAG", "package_ndc": "63621-356-20", "marketing_start_date": "20091014"}, {"sample": false, "description": "12 BOTTLE, PUMP in 1 BOX (63621-356-25)  / 236.6 mL in 1 BOTTLE, PUMP", "package_ndc": "63621-356-25", "marketing_start_date": "20091014"}, {"sample": false, "description": "4 BAG in 1 BOX (63621-356-40)  / 1000 mL in 1 BAG", "package_ndc": "63621-356-40", "marketing_start_date": "20251016"}, {"sample": false, "description": "473.2 mL in 1 BOTTLE, PUMP (63621-356-50)", "package_ndc": "63621-356-50", "marketing_start_date": "20200629"}], "brand_name": "SunDrops 75", "product_id": "63621-356_435330fc-c021-151b-e063-6394a90a229b", "dosage_form": "GEL", "product_ndc": "63621-356", "generic_name": "Alcohol", "labeler_name": "Sunburst Chemicals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SunDrops 75", "active_ingredients": [{"name": "ALCOHOL", "strength": ".6 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20091014", "listing_expiration_date": "20261231"}