act kids berry blast
Generic: sodium fluoride
Labeler: chattem, inc.Drug Facts
Product Profile
Brand Name
act kids berry blast
Generic Name
sodium fluoride
Labeler
chattem, inc.
Dosage Form
RINSE
Routes
Active Ingredients
sodium fluoride .5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
41167-0976
Product ID
41167-0976_e74290ff-fedb-4273-8c34-d2b044cbd452
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M021
Listing Expiration
2027-12-31
Marketing Start
2026-02-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
411670976
Hyphenated Format
41167-0976
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
act kids berry blast (source: ndc)
Generic Name
sodium fluoride (source: ndc)
Application Number
M021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/mL
Packaging
- 500 mL in 1 BOTTLE, PLASTIC (41167-0976-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e74290ff-fedb-4273-8c34-d2b044cbd452", "openfda": {"unii": ["8ZYQ1474W7"], "rxcui": ["240698"], "spl_set_id": ["4f81ea98-5c74-4473-9764-3f11d627cdf1"], "manufacturer_name": ["Chattem, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (41167-0976-0)", "package_ndc": "41167-0976-0", "marketing_start_date": "20260201"}], "brand_name": "ACT Kids Berry Blast", "product_id": "41167-0976_e74290ff-fedb-4273-8c34-d2b044cbd452", "dosage_form": "RINSE", "product_ndc": "41167-0976", "generic_name": "Sodium Fluoride", "labeler_name": "Chattem, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACT Kids Berry Blast", "active_ingredients": [{"name": "SODIUM FLUORIDE", "strength": ".5 mg/mL"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260201", "listing_expiration_date": "20271231"}