aquasoothe

Generic: aquasoothe

Labeler: dynarex corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name aquasoothe
Generic Name aquasoothe
Labeler dynarex corporation
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

petrolatum 41 g/100g

Manufacturer
Dynarex Corporation

Identifiers & Regulatory

Product NDC 67777-555
Product ID 67777-555_45878c3c-d05e-984c-e063-6294a90a4661
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M016
Listing Expiration 2026-12-31
Marketing Start 2025-12-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67777555
Hyphenated Format 67777-555

Supplemental Identifiers

RxCUI
725145
UPC
0616784146522 0616784146416 0616784146317
UNII
4T6H12BN9U

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 aquasoothe (source: ndc)
Generic Name aquasoothe (source: ndc)
Application Number M016 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 41 g/100g
source: ndc
Packaging
  • 24 TUBE in 1 CASE (67777-555-02) / 106 g in 1 TUBE (67777-555-01)
  • 12 JAR in 1 CASE (67777-555-04) / 396.9 g in 1 JAR (67777-555-03)
  • 12 BOX in 1 CASE (67777-555-06) / 144 PACKET in 1 BOX (67777-555-05) / .9 g in 1 PACKET
source: ndc

Packages (3)

Ingredients (1)

petrolatum (41 g/100g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45878c3c-d05e-984c-e063-6294a90a4661", "openfda": {"upc": ["0616784146522", "0616784146416", "0616784146317"], "unii": ["4T6H12BN9U"], "rxcui": ["725145"], "spl_set_id": ["45878c3c-d05d-984c-e063-6294a90a4661"], "manufacturer_name": ["Dynarex Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TUBE in 1 CASE (67777-555-02)  / 106 g in 1 TUBE (67777-555-01)", "package_ndc": "67777-555-02", "marketing_start_date": "20251216"}, {"sample": false, "description": "12 JAR in 1 CASE (67777-555-04)  / 396.9 g in 1 JAR (67777-555-03)", "package_ndc": "67777-555-04", "marketing_start_date": "20251216"}, {"sample": false, "description": "12 BOX in 1 CASE (67777-555-06)  / 144 PACKET in 1 BOX (67777-555-05)  / .9 g in 1 PACKET", "package_ndc": "67777-555-06", "marketing_start_date": "20251216"}], "brand_name": "AquaSoothe", "product_id": "67777-555_45878c3c-d05e-984c-e063-6294a90a4661", "dosage_form": "OINTMENT", "product_ndc": "67777-555", "generic_name": "AquaSoothe", "labeler_name": "Dynarex Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AquaSoothe", "active_ingredients": [{"name": "PETROLATUM", "strength": "41 g/100g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251216", "listing_expiration_date": "20261231"}